1.ApplicationNumber: US-17926361-A
1.PublishNumber: US-3175980-A
2.Date Publish: 19650330
3.Inventor: DAGLISH ANTHONY FENWICK
VONDERWAHL RODOLPHE
TILLOTSON GEORGE ARNOLD

4.Inventor Harmonized: FENWICK DAGLISH ANTHONY()
RODOLPHE VONDERWAHL()
ARNOLD TILLOTSON GEORGE()

5.Country: US
6.Claims:

7.Description:
(en)United States Patent The invention concerns a process for the improvement of the appearance in daylight of more or less colorless or white carriers by incorporation therein of slight amounts of the 3.5-bis-(sec. amino)-pyrazine-2.6-di-.
carboxylic acid amides obtained according to the new production process which, in UV-containing light, fluoresce violet-blue, blue to green blue.
Up to now only a few processes are known for the production of 3 .2;5.6-bis- (2.4-dioxo-1.2.3.4'-tetrahydro)-l.4-pyrimidino]-pyrazines which have been given the common name of bis-alloxazines. According to the literature these processes only give poor yields because of the side reactions which occur and because of the often troublesome purification of the crude products due to these side reactions. Thus for example, Bredereck et al. (Berichte der deutschen chemischen Gesellschaft, vol. 86, page 845 (1953) disclose yields of at most 45% of the theoretical for the condensation of 2 molecules of 1.3-dimethyl-4,5-diamino-uracil in mineral acid solution while splitting off ammonium salt, or in vol. 87 page 1268 (1954) give the same yields for the condensation of one molecule of 1.3-dimethyl-4.5- diamino-uracil with one molecule of 1.3-dimethyl-al1oxan. Also Timmis in US. Patent No. 2,581,889 mentions yields of up to 63% of crude 3.2;5.6-bis-[(1.3'-dimethyl- 2'.4' dioxo 1.2.3.4 tetrahydro) 1.4 pyrimidino1- pyrazine (also called 1.3.1.3'-tetramethyl-bis-alloxazine) for the condensation of one molecule of 1.3-dimethy1- 4-amino-5-nitroso-uracil with one mol of 1.3-dimethyl barbituric acid.
It has now been found that very good yields of 3.5- diamino-pyrazine 2.6 dicarboxylic acid derivatives are obtained if one mol of 1.3-disubstituted 4-amino-uracil is condensed with 1 mol of 1.3-disubstituted 4-amino-5- nitroso-uracil while splitting off one mol of water and one mol of ammonia to form the corresponding 3.2;5.6- bis [(2 .4' dioxo l.2.3.4' tetrahydro) l'.4' pyrimidino1-pyrazine and this compound is saponified by known methods either direct or in steps to form derivatives of 3.5-diaminopyrazine-2.6-dicarboxylic acid, if desired while modifying free carboxylic groups by ami' dation.
The good yields obtained in the said process are chiefly due to the fact that the new condensation of 1.3- disubstituted 4-amino-uracils with 1.3-disubstituted 4-amino-S-nitroso-uracils to form 3.2;5.6-bis-[(2.4'-dioxo- 1.2'.3'.4' tetrahydro) 1.4' pyrimidine] pyrazines, which is performed advantageously in polar organic solvents with an acid reaction and preferably in lower fatty acids, in particular in glacial acetic acid, proceeds more uniformly than the known processes.
Good yields of up to 90% of the theoretical of these valuable intermediate products are obtained and this in contrast to the syntheses mentioned even when the nitrogen atoms of the uracils are substituted by higher organic radicals than methyl groups. Also the 3.2;5.6-bis- 3,175,9 0 Patented Mar. 39, 1965 ice dinol-pyrazines variously substituted at the nitrogen atoms of the two tetrahydropyrimidine rings are obtainable in good yields according. to the new process. That the starting materials used according to the said process would condense so favorably was surprising in view of atom. As nitrogen substituents both hydrocarbon radicals and'also substituted hydrocarbon radicals of the aliphatic, araliphatic, alicyclic, or aromatic series are used, for example, methyl, ethyl, n propyl, isopropyl, n-butyl, hydroxyethyl, methoxyethyl, ethoxyethyl, -methoxypropyl, benzyl, chlorobenzyl, methylbenzyl, cyclohexyl, methyl-cyclohexyl, phenyl, methylphenyl, chlorophenyl, methoxyphenyl groups and starting materials having the same or different substituents at the nitrogen atom can be condensed.
Saponification of 3.2;5.6-bis-[(2'.4-dioXo-1.2.3.4-tetrahydro)-l'.4-pyrimidino]-pyrazines in aqueous, alcoholic or organic/aqueous solution or suspension, with alkalies such as sodium or potassium hydroxide, leads to the corresponding 3.5-bis-(sec. amino)-pyrazine-2.6-dicarboxylic acid amides. Under more vigorous conditions, for example in ethanolic potassium hydroxide, the 3.5-bis-(sec. amino)-pyrazine-2.6-dicarboxylic acid monoamides are formed. In these compounds the free carboxyl group can be converted with thionyl chloride into the carboxylic acid halide group. Aminolysis of this group leads to the acid amides. A technically particularly simple method of performing the amidation consists in dissolving the carboxylic acid and the amine to be introduced in a strong tertiary nitrogen base such as pyridine, homologous pyridines or triethylamines and then stirring in gradually the necessary amount of thionyl chloride or phosphorus trichloride or bromide in the cold. After removal of the nitrogen base by dilution with water or steam, the 3.5-diaminopyrazine-2.6-dicarboxylic acid diamide is obtained direct. The free carbonyl group, which may be in the form of its salts, can also be esterified, for example on treating with dialkyl sulphates.
Other derivatives can be obtained in the aminolysis of the acid chloride group by using amines which contain different substituents from those originally at the nitrogen atom which was linked to the carbonyl group. In this way, in particular also aromatic and heterocyclic amine radicals can be introduced, for example phenylamino, methylphenylamino, chlorophenylamino, methoxpyhenylamino, pyridyl-(2)-amino and morpholino groups. However, it is also possible to introduce hydroxy-alkylamino groups in this way, for example the monoethanolamide, diethanolamide, 2-hydroxypropylamide group, also aminoalkyl carboxyl acid, carboxylic acid ester and carboxylic acid amide groups. Even urea and substituted urea groups, e.g. the monophenyl urea group can be introduced in this way.
However, also unsymmetrical amidated end products can be obtained by aminolysis of 3.2;5. 6-bis-[(2'.4-dioxo 1'.2'.3'.4 tetrahydro) pyrimidino 1'.4] pyrazines at a higher temperature with amines such as e.g. benzylamine, whereby only one dioxo-tetrahydro-pyrimidino ring is split, and then further hydrolysing with alkalies.
4 There are, thus, several methods by which it is possible to vary at will the substitution of a diaminopyrazine dicarboxylic acid amides according to the desired intended use. H 5
' 0.9 The. following sequence illustrates the reactions described:
radical, in particular the radical of a primary amine are particularly valuable because of their violet-blue, blue to green-blue fluorescence. In the above sequence of reactions, R R R R R R and R, can represent the a same or different organic radicals which have no dyestuf character; R and R; can represent in addition, hydrogen.
R R R R represent preferably aliphatic radicals such as alkyl and substituted alkyl groups, for example methyl, ethyl, n-propyl, n-butyl, hydroxyethyl, B-hydroxypropyl, methoxyethyl, ethoxyethyl groups, however, they may also represent aralkyl'and substituted aralkyl groups such as benzyl, methylbenzyl, chlorobenzyl, methoxybenzyl groups or cycloaliphatic radicals such as cyclohexyl, 'methyl-cyclohexyl groups. R and R can be hydrogen or the same as R in addition R, can also be a heterocyclic radical, for example the Z-pyridyl radical or a'divalent radical linking two. pyrazine radicals, for
example an alkylene or a diphenyl alkane radical;
it can also represent a carbamyl radical, for example the phenyl carbamyl radical and thus X can also represent a urea radical or a ureido radical which may possibly be organically substituted. R and R together With the carbarnide-N- atom can also represent a heterocyclic radical, for example a piperidino or a morpholino group.
Because of their fluorescence in ultraviolet light and in daylight, the 2.5-di-(sec. amino)-pyrazine-2.6-dicarboxylic acid derivatives of the Formula IV wherein X represents an amine radical, in particular the radical of a primary amine, are suitable for improving the appearance of more or. less colorless carriers by optically compensating the yellowing thereof by the violet-blue, blue to green-blue fluorescence. For this purpose, slight amounts thereof, for example amounts of 0.001 to 1% of the carrier, are incorporated into the material to be brightened. By carriers are meant substances from the class of natural and synthetic polypeptides such as wool, silk, polyamide fibres, polyurethane fibres; vinyl polymers such as polyvinyl chloride, polyacrylic acid esters, polystyrene, polyethylenes, unsaturated polyesters; cellulose acylates such as cellulose acetates to cellulose triacetate; also cellulose nitrates, e.g. in the form of Zapon varnishes. The 2,.5-di-(sec, amino)-pyrazine-2.6-dicarboxy1ic acid 4 derivatives can also be used as additives to cosmetic preparations, for example in lipstick and creams. They can be incorporated into carbohydrates such as starches, or fats and waxes as Well as parafiines.
The following examples illustrate the invention. Where not otherwise stated, parts are given as parts by weight. The temperatures are in degrees centigrade; The relationship of parts by Weight to parts by volume is as that of kilogram to liters.
Example 1 3.S-bis-ethylaminopyrazine 2.6 dicarboxylic acid-bisethylamide of the formula:
C I-h-NH- C O -L V 212 parts of 1.3 diethy1-4-amino-5-nitroso-uracil and 183 parts of l.3-diethyl-4-amino-uracil are dissolved in 7 50 parts of glacial acetic acid and the solution is refluxed for 3 hours While stirring. The grey-greenish solution is cooled, the precipitate formed is filtered off under suction, washed well with water and dried. 320 parts of 3.2;5.6-bis[(1'.3'-diethyl-2T.4-dioxo-1.2'.3.4'- tetrahydro)-1.4-pyrimidino]-pyrazine are obtained as white crystals which melt at 233.5-234.5. This corresponds to a yield of 89% of the theoretical calculated on the 1.3-diethyl-4-amino 5-nitrosouracil used. An analytically pure preparationrecrystallized from acetic acid which melts at 235.5-236 has the following elementary analysis:
Calculated for C H O N C=53.32%; H=5.59% N=23.32%. Found: C=53.l7%; H=5.61%; N =23.11%.
To saponify the 3.2;5.6-bis-[(1'.3'-diethy1-2.4'-dioxo- 1'.2.3.4-tetrahydro)-1.4-pyrimidino]-pyrazine, 10 parts are refluxed for 2 /2 hours with 300 parts by volume of 1 N-caustic soda lye and 200 parts of ethanol. The precipitate which crystallizes out on cooling is filtered'ofi under suction, well Washed and dried.
7.5 parts of 3.S-bis-ethylamino-pyrazine-2.6-dicarboxylic acid-bis-ethylamide (MP. 133-134") are obtained. An analytically pure preparation recrystallized from ethanol, has the same melting point and the following elementary analysis:
Calculated for C H O N C=54.52%; H==7.84%; N:27.25%. Found: C=54.63%; H=8.00%;
On using the corresponding amountsof 1.3-dipropyl-,
1.3-dibutyland 1.3-dimethyl-4-imino-uracil and of 1.3- dipropyl, 1.3-dibutyland 1.3-dimethyl-4-amino-S-nitrosouracil, the following 3.2;5.6-bis-[(l.3'-dialkyl-2'.4'-dioxotained in a similar manner:
By saponifyingthese according to paragraph 2 of the example, the corresponding 3.5-bis-alkylaminopyrazine-2.6- dicarboxylic acid-bis-alkylamides are obtained:
M Elementary analysis, percent Alkyl degrees i i C C H H N N cald found cald found cal'd found 11-G H1 96-97 59. 31 59.43 i 8.85 8. 91 n-CaHo. 89-91 (0 CH3 232-233 47. 6 47. 8 6. 35 6. 04 33.3 33. 5
1 The crystals contain crystal solvent.
All these 3.5 bis alkylaminopyraZine-Z.6-dicarboxylic acid-bis-alkylamides have a strong to very strong violetblue fiuoresence depending on their composition. Because of this property they can be used as follows for improving the appearance of vinyl polymers:
(a) Polyvinyl chloride.-0.07 partsof 3.5-bis-methylaminopyrazine-Z.fi-dicarboxylic acid-bis-rnethylamide are added to 67 parts of polyvinyl chloride powder, 33 parts of dioctyl phthalate, 2 parts of di-n-butoxy tin dilaurate and 0.3 parts of sodium penta-octyl tripolyphosphate, the mixture is worked on a set of mixing rollers for 15 minutes at 160 and then drawn out into foils. The foils so produced have a more white appearance in daylight than those produced without a content of dialkylaminopyrazine dicarboxylic acid alkylamido. Opaque, white polyvinyl chloride foils of greatly improved appearance are obtained if 7 parts of titanium dioxide (Anatas) areadded to the above mixture.
The 3.5-bis-ethylamino-, 3.5-bis-propylaminoand 3.5- bis-butylaminopyrazine-2.6-dicarboxylic acid bis-ethyl-, or -propylor -butylamides described in the above example can be used in the same manner with the same success.
(b) Polystyrene.---l00 parts of polystyrene powder are thoroughly mixed with 0.003 parts of 3 .5 -'bis-methylaminopyrazine-2.6-dicarboxylic acid-bis-methylamide and the mixture is then homogenised on a set of mixing rollers at 130. The hard plates obtained are broken up and further worked up on an injection moulding machine or in presses. Objects having a much more white appearance in daylight than those produced without the addition of 2.S-bis-alkylaminopyr-azine-2.G-dicarboxylic acid bis alkamides are obtained.
Opaque objects of improved appearance are obtained if 2 parts of titanium dioxide (Anatas) are added to the above mixture. The 3.5-bis-ethylamino-, 3.5-bis-propylaminoand 3.5-bis-butylaminopyrazine-2.G-dicarboxylic acidbis-ethylamides, -bis-pyropylamides, or -bis-butylamides also described in the above example can be used in the same manner and with similar success.
I (c) .Polyethylene.0.05 parts of 3.5-bis-propylaminopyrazine-Z.G-dicarboxylic acid bis-propylamide are mixed dry at room temperature with 100 parts of high pressure polyethylene in granulate form and the mixture is then worked into a tube in the extruder at 120l30. The objectis considerably more white than that produced without brightening agent.
To produce opaque polyethylene, 0.1 parts of 3.5-bispropylaminopyrazine-Z.6-dicarboxylic acid-'bis-propylamide, 2 parts of titanium oxide and parts of polyethylene granulateare mixed and pressed at-130".
A material is obtained in this way which has a considerably more white appearance in daylight than that produced without brightening agent. The 3.5-bis-ethylamino-,
3.5-bismethylaminopyrazine-2.6-dicarboxylic acid-bisethyl or -methyl amides described in the above example can be used, in the same manner and with similar success.
(d) Polymethacrylic acid methylester.0.004 parts of then temperedfor 1 hour at Because of its very beautiful blue-violet:fiuorescence, the glass clear resinous body obtained has amore brilliant appearance in daylight than a non brightened material.
If the brightening agent used is replaced by the same amount of the 3.5-bis-ethylaminoor 3.5-bis-proplyaminopyrazine-2.6-dicarhoxylic acid-bis-ethylor -propylamides described in the above example, then similar beautifully brightened products are obtained. i (e) Acetyl cellulose-0.2 parts of 3.5-=bis-ethylaminopyrazine-2.6-dicarboxylic acid-bis-ethylamide, 25 parts of diethyl phthalate and 75 parts of acetyl cellulose are dis solved in 900 parts of acetone. The solution is poured onto glass plates and, after evaporation of the acetone, a transparent film is obtained. In daylight this film appears much more brilliant than a corresponding film produced without the addition of brightening agent.
Opaque cellulose acetate films are obtained if. 5 parts of titanium dioxide (Anatas) are added to the above mixture before it is poured ontothe glass plates The opaque films obtained are much more white indaylight than comparative samples produced without brightening agents.
The '3.5-bis-methylamino-, 3.5-bis-propy1amino and 3.5-bis-butylaminopyrazine-2.6-dicarboxylic acid-bismethylor -propyl or -butyl amides described in the above example can be used in the same manner with the same success.
if, in the first paragraph under (e) of this example, the diethyl phthalate is not added, then a solution in acetone is obtained which produces cellulose fibres of greatly improved appearance in the dry spinning process.
The appearance of cosmetics can also be improved with the 3.S-bis-alkylaminopyrazine2.6-dicarboxylic acid-bisalkylamides as follows:
(f) Creams-A cold cream of dazzling white appearance is obtained if 0.1 parts of 3.5-bis-methylaminopyrazine-2.6-dicarboxylic acid-bis-methylamide are dissolved in 25 parts of cetyl alcohol and this solution is mixed homogenously in the mixing apparatus with 55 parts of paraflin oil, 10 parts of bleached beeswax and 10 parts of wool fat (anhydrous).
Similar creams are obtained if, instead of the brightening agent mentioned, the 3.5-bis-ethylaminoor 3.5-bispropylamino-pyrazine-2.6-dicarboxylic acidbis-ethyl or -propyl amides mentioned in the above example are used.
Because of their favorable shade of fluorescence and their afiinity, these 3.S-bis-alkylaminopyrazine-2.6-dicarboxylic acid-bis-alkylamides are also suitable for the optical brightening of natural and synthetic polypeptide fibres according to the application methods described in Examples 2 and 3.
Example 2 3-propylamino-5-ethylamino-pyrazine-2-carboxylie acid propylamide-6-carboxylic acid ethylamide of the formula:
cooled and diluted with water. The precipitate formed is filtered off under suction, washed well with water and dried. 70 parts of 3.2-[(l'.3' diethyl 2'.4' dioxo- 1'.2'.3.4-tetrahydro)-1'.4'-pyrimidino] 5.6- l'.3'-dipro .pyl-2'.4-dioxo-1'.2.3.4'-tetrahydro)-l'.4' pyrimidino] pyrazine are obtained in the form of white crystals which melt at 147.5-149". This corresponds to a yield of 90% of the theoretical, calculated on the 1.3-diethyl-4-arnino-5- ntroso-uracil used. An analytically pure product recrystallised from ethanol melts at 150-151" and has the following elementary analysis:
' Calculated for C d-1 N 0 2 Found .C=55.70%; H=6.52%.
parts are refluxed for 2% hours with 300 parts by volume of 1 N-caustic soda lye and 200 parts of ethanol. The reaction mixture is cooled and then neutralised with diluted hydrochloric acid. The precipitate formed is filtered ofi under suction, Washed and dried. 7.2 parts 0153- 25 propylamino-5-ethylamino-pyraZine-2.6-dicarboxylic acid- '2 propylamide-6-ethylamide are obtained. M.P. 91 923 An analytically pure preparation recrystallised from ethanol has the following elementary analysis:
Calculated for C H N O C=57.12%; H=8.39%; 30
On condensing 4-amino-uracils with 4-amino5-nitroso-' Found C=57.l4%; H=8.45%;
uracils which are differently alkyl substituted at the ring nitrogen atom, for example by using corresponding amounts of l.3-dimethyl-, 1.3-diethyland 1.3-dipropyl- 4-amino-uracils and l.3-dimethyl-, 1.3-diethy1- and 1.3-
'1 and 6.005 part of 3-propylamino-5methylaminopyrazine-Z-car'ooxylic acid-propylaniide--carboxylic' acid methylamide. The fabric is then rinsed and dried in the air. The fibres so treated have a much more White appearancein daylight than untreated goods. 1
The 3 -methylamino-5-ethylamino-pyraZine-2-carboxylic acid-methylamino-6-carboxylic acid ethylamide and 3-- propylamino S-ethylamino-2-carboxylic acid-propylamide-6-carboxylic acid ethylamide described in the above example can be used in the same way with similar success.
flannel are washed for half anhour at in 2000 parts of a washing liquor containing 5 parts of an alkylaryl sulphonate of the marketed name Santomerse No. 1 and 005 parts of 3-propylamino-5-ethylamino pyrazine-2-carboxylic acid-propylamide-6-carboxylic acid-ethylamide.
The Wool is then rinsed and dried in the air. 'In this way" wool of a considerably more white appearance is obtained than when the wool is washed without the addition of the brightening agent. 7
The 3-propylamino-5-methylamino-pyrazine-2-carboxylic acid-propylamide-6-carboxylic acid methylamide and 3 methylamino-5-ethylaminopyrazine-Z-carboXylic acid methylamide-G-carboxylic acid ethylamide described in.
dipropyl 4-amino-S-nitroso-uracils, the following unsymmetrical 3.2 ;5.6-[1'.3'-dialkyl-2.4'-dioxo-112C314 7 tetra CHPNH-C hydro)-l'.4'-pyrimidino]-pyrzaines are obtained in the 49 CH3-NH-'fi-C CGNH I I same way. N l
. Elementary analysis, percent Lalkyl 2.alkyl M.P.. R18! R2 R3 & R; degrees C cald 0 found H eald H found N cald N found CH3 n-C H 169-163. 5 53.32 53.36 5.59 5. 57 23.32 23.24 CH O2H 253254 50.60 50. 01 4.85 4.72
On saponifying these according to paragraph 2 of the above example, the corresponding unsymmetrical l.3-bisalkylamino-pyrazine-2.6-dicarboxylic acid-bis-alkylamides are obtained:
31 parts of 1.3-dimethyl-4-amino-uracil and 40 parts of 1.3-dimethy1-4-amino-5-nitroso-uracil are refluxed while stirring for 3 hours in 200 parts of glacial acetic acid. The reaction mixture is cooled, the precipitate formed is Elementary analysis, percent Lalkyl 2.alkyl M.P., R & R7 R & R degrees C eald 0 found H cald 11 found N eald N found OH n-G H 136-137 54. 52 54. 64 7. 84 8. 02 27. 25 26. 98 CH CZH 169-170 51. 41 51. 66 7. 19 7. 17 29. 98 29. 95
7 All these unsymmetrical 3.5-bis-alkylamino-pyrazine- 2.6-dicarboxylic acid-bis-alkylamides have. a strong to very strong violet-blue fluorescence depending on their composition; Due to this property, they can be used for the brightening ofnatural and synthetic polypeptides as 70 follows:
(a) Synthetic p0lypeptides.-50 parts of pale yellowish Nylon fabric are washed for 30 minutes at 70 in 2500 parts of a washing liquor containing 6.3 parts of an alkylaryl sulphona-te of the marketed name Santomerse No. 7
filtered oil? under suction, washed Well with water and dried. 51 parts of 3.2;5.6-bis-[(1'.3'-dimethyl-2'.4'-dioxo- 1' .2 .3.4-tetrahydro 1 .4'-pyrimidino] -pyrazine are obtained in the form of white crystals which melt at 390 (the melting point depends on the heating time). This corresponds to a yield of 84% of the theoretical, ca1culated on the 1.3-dimethyl-4-amino-uracil used. Recrystallised from acetic acid, an analytically pure preparation has the following elementary analysis: 7
Calculated for C H O N C=47.4%; H=4.l7%;
(b) WOOL- parts of previously bleached wool N=27.8%. Found: O=47.4%; H=3.95%; N;27.6%.
To saponify the 3.2;5.6-bis-[(1'.3-dimethyl-2'.4-dioxo- 1'.2.3'.4 tetrahydro) 1'.4'-pyrimidino]-pyrazine, 152 parts are refluxed for 6 hours with a solution consisting pants of aniline and 400 parts of abs. pyridine, which i solution is cooled with a mixture of ice/ sodium chloride See footnote at end of table.
of 200 parts of potassium hydroxideand 2400 parts of 5 and washed well with water. Pale yellow crystals of ethanol. 117 parts of 3.5 bis-methylamino-2-carboxy- 3.S-bis-rnethylamino-pyrazine-Z-carboxylic acid phenyl-; pyrazine-S-carboxylic acid methylamide (M.P. 214, deamide-6-carboxylic acid methylamide are obtained which composition dependent on the heating time) are obtained. melt at 195-197 Recrystallised from ethanol, an analytically pure prepa- Recrystallised from ethanol, an analytically pure prepration has the following elementary analysis: 10 aration melts at 198-1985 and has the following ele- Calculated for C H O N /2H O: C=43.48%; mentary analysis: H=5.68%;N-=28.3%. Found: C=43.59%;H==5.50% Calculated for C H O N C=57.31%; N=5.77%; N=28.45%. N=26.74%. Found C=57.42%; N=6.01%; N=
To amidate the 3.S-bis-methylarnino-2-carboxypyraz- 26.86%. ine-G-carboxylic acid methylamide 20 parts are mixed 15 Amidafion 0f y Y-PY with 150 parts of thionyl chloride. The mixture is left to y acid y fimide in pyridine or in an aquestand for minutes and then the excess thionyl chloride ous medium according to paragraph 3 of this example is removed in the vacuum. The remaining crystalline with the amines correspo d ng to R in the following acid chloride is then slowly added to a solution of 10 table, pr the following Compclmds! CH NHC \C-NHCH3 CH NH-(J -C-R No. R M.P.,1 Colour of degrees fluorescence 1 NH2 290-292 Violet-blue.
2 -NHOHCH2OH 21o-21o.5 Do.
a NHGHCHz-CH: 218-219 Do.
4 NH-CH -OH3 197-19215 Lo.
5 NHCH2O 218.5-220 Blue-violet.
e -NHOHz-CH:-O 76-78 Do.
7 -NH 126.5427 Blue.
(SCH:
s '-NH-OHIOHzOH2-CH3 194 196 Violet-blue.
9 NHOOC: 252-254 Blue.
10 Nl1-CHz-OH=CH2 1944955 Violet-blue.
11 -NH-'(CHfl)7 CH3 121-121; Do.
CH2-CH2 12. -NH0 9H2 237-238.. Blue-violet.
CH3 13-.." N 128-129 VlOlGl].
CHa
CHz-CH 14 NH-O 188-190 Violet-blue.
HCCH
15 -NH-C 0-H 223-224 Blue-violet.
N==OH i 16 NH-(Il-CHa 204-205 Violet-blue;
17 NH-C "CHa 211- 2125 Blue-violet.
18... NH- 194-195 Do.
1 No. R M.P., Colour of degrees fluorescence 232-234 Do. 36"-.- -HN 1 The melting points depend greatly on the heating time.
1 The melting points depend greatly on the heating time. 1
On using corresponding amines of 1.3-dibenzyland 1.3-diethyl-4 amino-uracils and 1.3-dibenzyland 1.3-diethyl-4-amino-5-nitro-uracils, the 3.2;5.6-bis-[(1.3'-dibenzyl 2'.4' dioxo 1'.2'.3'.4' tetrahydro)-l'.4.- pyrimidino]-pyrazines and 3.2;5.6-bis[(l'.3'-diethyl- 2'.4'-dioxo-l.2'.3.4-tetrahydro) l'.4'-pyrin1idino]-pyrazines are obtained in the same manner. On saponifying these according to paragraph 2 of this example, the corresponding 3.5-bissubstituted aminopyrazine-2-carboxylic acid-6-carboxylic acid benzylor ethylamides are 3.5 bis methylamino pyrazine 2 carboxylic acid phenylamide-6-carboxylic acid methylamide and 0.2 parts of formic acid. After rinsing and drying, the fabric treated has a much more white appeaarnce in daylight than before treatment. 1 1
(2) 50 parts of undyed Nylon are Washed at 70 for half an hour ina washing liquor (liquor ratio 1:20) containing 0103 parts of 3.5-bis-methylaminopyrazine-Z-carboxylic acid-[3-methoxyphenylamide]-6-carboxylic acid methylarnide and 8 parts of dodecyl benzene sulphonate,
and then rinsed and dried. The Nylon so treated has a much more brilliant appearance in daylight than material washed without the addition of brightening agent. In-
. stead of dodecyl benzene sulphonate, also other synthetic washing and cleansing agents such as, for example, fatty alcohol sulphates or oleoyl tauric acid. alkali salts etc. can be used.
The following compounds described in the above tables can be used in the same manner with similar success instead of the brighteningagents mentioned: Nos. 1, 2, 3, 4, 5, 6, 8, 10, 11, 12, 14, 15, 16, 19, 20, 21, 22, 23, 24, 25, 26, 27, 29, 30, 31, 33, 34, 36, 38, 39, and 41.
(b) W00l.-(1) 25 parts of white woolen knitted goods are treated in a dyebath (liquor ratio 1:30) for half an hour at 50-55 which contains 0.02 parts of 3.5- bis-methylaminopyrazine-Z-carboxylic acid phenylamide- 6-carboxylic acid methylamide and 0.5 parts of formic acid. The goods are then rinsed and dried. The wool 1 so treated is clearly more White in daylight than untreated obtained. 40 wool.
Elementary analysis in percent Substituent M.P., R R and R degrees 1 C cald 0 found H cald H found N cald N found -CH7 161-162 69.36 69. 30 5.39 5.36 14.98 15.06 C1Hs 174-175 51. 23 51.32 6.81 7. 02 24. 90 25.08
By amidation in pyridine according to paragraph 3 of (2) parts of previously bleached wool flannel are this example, the corresponding 3,5-bis-ethyl-or -benzyl treated for 1 hour at 5055 in a dyebath (liquor ratio aminopyrazine-2-carboxy1ic acid ethylor benzylamide- 1:20) containing 3 parts of sodium hydrosulphite and 1 G-carboxylic acid amides are obtained, for example: part of sodium pyrophosphate and also 0. 05 parts of 3.5-
Substitu- Elementary analysis in percent No. ent R1,Rz X M.P.,
and Rs degrees C eald 0 found H cald H found N cald N found 40..w 02H5 NH@ 14115-1415 60.65 60.77 6.79 7.07 23.58 23.55
41... (Jim -NHC 108-109 56.9 56.6 6.7 6.7 26.6 26.6
1 E HG CH (a) Synthetic p0lypeptides.(1) 10 parts of a paleyellowish Nylon fabric are treated for 30 minutes at inadyebath (liquor ratio 1:40)coi1taining 0.01'parts of used inthe'same'rnanner with the same success: Nos. 1,2,
bis-methylaminO-pyraZine-Z-carboxylic acid phenylamide- 70 6-carboxylic acid methylarnide. After rinsing and drying,
The following compounds in the above tables can be 3, 4, 5, 6, 7, 8, 10, 11, 12, 14, 15, 16, 18, 19, 21, 22 23, 24,25, 27, 29, 30, 31, 39, 40 and 41.
i Pure silk.10 parts of pale yellowish pure silk are washed at 55 for 30 minutes in 200 parts of a washing The compound melts at 160162' (th Recrystallised from methanol, an analytically pure [preparation has the following elementary analysis:
liquor containing 0.5 parts of an alkylaryl sulphonate of Calculated for C H 0 N 'C 49.43%; H=6.41%; the marketed name Santome'rse No. 1 and 0.01 parts N=26.20%. Found: C=49.99%; H=6.49%; N: of 3.5-bis methylamino-pyrazine-Z-carboxylic acid phen- 26.27%. a ylamide-r6-carboxylic acid methylamide, and then rinsed To amidate the 3-methylamino-3-ethylamino-pyr i and dried in the air. In this way, pure silk of consid- Z-carboxylic acid-6-carboxylic acid ethylamide, 20 parts erably more'white apparance is obtained than if it had 10 of this compound are mixed with 100 parts of thionyl been washed without the addition of the brighten ng chloride. Themixture is left to stand for 45 minutes agent named. and then excess thi-onyl chloride is removed in the Also very beautiful effects are obtained if instead of vacuum. The acid chloride which remains is then poured the br ghten ng ag nt us d a t f l g into a solution of 300 parts of concentrated aqueouspounds mentioned in the tables are used NOS- 1, 2, ammonia and 100 parts of ethanol, which solution has 4, 5, 7, 11, 12, 15, 27 and 31. been cooled with a mixture of ice and sodium chloride. Acetate P s Of ac t Silk fabric a The whole is stirred overnight. The precipitate formed treated at 7 for 30 minutes in a bath q ratio is filtered off under suctionand washed Well with water. 1:30) containing 0.0025 parts of 3.5-bis-methylamino- 3 methylamino-5-ethylamino-pyraZine-2-carb0Xylic acid pyrazine-Z-carboxylic acid phenylamide-6-carboxylic acid amide-6-carboxylic acid ethylamide is obtained in the methylamide- After rinsing and drying, the fabric has v form of pale yellow crystals which melt at 212-'214. a considerably more white appearance than before treat- Recrystallised from ethanol, an analytically pure prepment. aration melting at 223234 has the following elementary The following compounds described in the above analysis:
tables can be used in the same manner with similar suc- Calculated for C H O N C==49.6l%; H=6.81%; cess instead of the brightening agent mentioned: Nos. N=31.56%. Found: C=49.49%; H=6.90%; N= 1, 2, 3, 4, 5,6, 7, 8, 10, 11, 12, 14, 15, 16, 18, 19, 20, 31.88%. 21, 22, 23, 26, 27, 29, 31, 33, 35, 39, 40 and 41. The following 3-methylamino-5-ethylamino-pyrazine- (e) Cellulose triacetate.-10 parts of cellulose tri- Z-carboxylic acid alkylamide-6-carboxylic acid ethylacetate silk fabric are treatedfor half an hour in a dye- 30 amides for example are obtained in the same manner bath on a boiling water bath, the dyebath liquor ratio on amidation with other amines:
Alkyl My lementary analysis in percent degrees C cald 0 found H cald H found N cald N found --CzHs 162-164 53.04 53.06 7. 53 7.59 28.55 28.53
-oan7 84-86 53. 3 53. 4 7. 85 7. 9s 26. 7 20. s
being 1:30 and containing 0.005 parts of 3.5-bis-methyl- Depending on their composition, all these 3-methylaminopyrazine 2 carboxylic acid phenylamide-6-caramino-5-ethylamino-2-carboxylic acid alkylamide-6-carboxylic acid methylamide. After rinsing and drying, the boxylic acid ethylamides have a strong to very strong fabric has a much more brilliant appearance than before violet-blue fiuoroescence. Because of this property they treatment. canbe used for the brightening of natural as well as syn- Instead of 3.5-bis-methylamino-pyrazine-Z-carboxylic thetic polypeptide fibres. acid phenylamide-6-carboxylic acid mcthylamide, the fol- Wool treated in an acid bath according to paragraph lowing compounds described in the above tables can be (b) of Example 3 or in a neutral bath according to paraused in the same way with similar success: Nos. 1, 2, 3, graph (b) of Example 2 has a considerably more White 4, 5, 7, 11, 12, 15, 27 and 31. appearance than untreated wool.
The compounds described in the above Example 3 are Nylon treated in an acid bath according to. paragraph also very well suited for the brightening of synthetic (a) of Example 3 has a much more white and luminous materials and cosmetics, the procedure being as described appearance than before treatment. in Examples 1 and 2. Also fibres made up from cellulose acylates can be Example 4 beautifully brightened with these unsymmetrical pyrazine 3 farts; reassessment stains? acid annde-6-carboxyl1c acid ethylannde of the formula. graph (d) of Example 3 than untreated fabric.
Such 3 methylamino 5 ethylamino 2 carboxylic O,H -NHO C-NH-CH acid alkylamide-6carboxylic acid methyl amides are also C2H5 NH G suitable however for the brightening of vinyl polymers I] because of their intensive fluorescence. Thus for ex- O N O ample, polyvinyl chloride foils produced according to T0 p y the Y paragraph (a) of Example 1, have a much more white tetrahydfo) '-PY appearance in daylight than such foils which contain no ethyl 2'.4' dioxo 1'.2'.3.4'-tetrahydro)-1'.4'pyrimib i h i agent dinol-pyrazine, produced for example as in Example 2, Example 5 57 parts'of this compound are refluxed for 6 hours with a solution consisting of 45 parts of potassium hydroxide 0.075 parts of 3.5 bis methylamino pyrazine 2- and 500 parts of ethanol. The ethanol is distilled off, carboxylic acid-phenylamide-G-carboxylic acid methylthe reaction mixture is acidified with diluted hydrochloric amide are worked into 100 parts of soap powder consistacid and 43 parts of 3-methylamino-S-ethylaminoing of the sodium salt of fatty acids with 5% water conpyrazine-Z-carboxylic acid-G-carboxylic acid ethylamide tent. Nylon fabric washed at 40 in a washing liquor 17 (liquor ratio 1:30) containing parts per litre of the soap powder described above, has a much more brilliant appearance.
If, in the above washing agent, 0.09 part of 3.5-bismethylamino-pyrazine 2.6 dicarboxylic acid methylamide are used instead of the pyraizne named, then the treated fibres also have a beautiful white appearance. If an even stronger brightening effect on acetate silk is required, then 1 to 2 parts of the brightening agent named can be used.
Example 6 0.075 part of 3.S-bis-methylamino-pyrazine 2 carboxylic acid phenylamide-6-carboxylic acid methylamide are worked into 100 parts of washing agent consisting of 55% sodium salt of lauryl alcohol sulphate, 40% sodium sulphate, 2% carboxymethyl cellulose and 3% water content.
Wool, as well as nylon and acetate silk fabric, which is washed at 40-50 in a washing liquor (liquor ratio 1:30) containing 5 parts per litre of the washing agent described above, has a beautiful white appearance.
If, instead of the pyrazine in the above anion active washing agent, 0.2 parts of 3.5-bis-methylamino-pyrazine- 2.6-dicarboxylic acid methylamide or 0.2 part of 3-propylamino-S-niethylamino-pyrazine-2-carboxylic acid propylamide-6-carboxylic acid methylamide or 0.15 parts of 3- ethylamino 5 methylamino pyrazine 2.6 dicarb oxylic acid ethylamide or 0.3 part of 3-propylmino-5- ethylamino-pyrazine 2 carboxylic acid propylamide-6- carboxylic acid ethylamide or 0.2 parts of 3-ethylamino-5 methylamino-pyrazine 2 carboxylic acid ethylamide- 6-carboxylic acid benzylamide are used, then similar effects are obtained on treating the fibres above mentioned.
Instead of the anion active washing agent described, also those consisting of salts of sulphonic acid esters of ethoxylated fatty alcohols or salts of sulphonic acid esters of alkanol amides of fatty acids can be used.
Example 7 0.05 parts of 3.5 bis methylamino pyrazine 2- carboxylic acid phenylamide-G-carboxylic acid methylamide are worked into 100 parts of washing agent of the composition: 20% dodecyl benzene sulphonate, sodium lauryl s'ulphonate, 2% carboxymethyl cellulose sodium lauryl sulphonate, 2% carboxymethyl cellulose, 15 tetrapyrophosphate, tripolyphosphate, 22% sodium sulphate and 6% water.
If nylon or acetate silk is washed at 60 in a washing liquor containing 6 parts per litre of the washing agent described, then the fabric has a brilliant appearance.
If, in the above washing agent instead of the pyrazine mentioned, 0.12 parts of 3.5 bis ethylamino pyrazine- 2.6 dicarboxylic acid methylamide are used, then the fibres mentioned also have a beautiful appearance.
If the washing agent contains 0.15 parts of 3.5-bismethylamino pyrazine 2 carboxylic acid pyridylamide- 6-carboxylic acid methyl amide, then wool flannel or acetate silk washed therein has a beautiful white appearance.
Example 8 0.2 parts of 3.5 bis methylamino pyrazine 2.6- dicarboxylic acid methylamide are incorporated into 100 parts of washing agent consisting of 45% soap, 5% water glass, 10% pyrophosphate, 15% sodium carbonate, 3% magnesium meta silicate, 7% perborate and 15% water.
Nylon and acetate silk fabric which are washed at 70 in a washing liquor (liquor ratio 1:30) containing 8 parts per litre of the above washing agent have a much more white appearance than when washed without the adidtion of the brightening agent.
If in the above washing agent, instead of the brightening agent named, 0.06 parts of 3.5-bis-methylamino-pyrazine- 2-carboxylic acid pyridylamide-G-carboxylic acid methylamide or 0.04 parts of 3.5-bis-methylamino-pyrazine-2- carboxylic acid phenylamide-6-carboxylic acid methylamide, are used, then similar effects on the above mentioned fibres are obtained.
Example 9 0.1 parts of 3.5-bis-ethylamino-pyrazine-2.6-dicarbox ylic acid ethylamide are incorporated into parts of washing agent of the composition: 12% dodecyl benzene sulphonate, 10% sodium lauryl sulphate, 5% water glass, 2% carboxymethyl cellulose, 15 tripolyphosphate, 20% pyrophosphate, 10% sodium carbonate, 20% sodium sulphate and 6% water.
Nylon fabric which is washed at 70 in a Washing liquor (liquor ratio 1:30) containing 8 parts per litre of the washing agent described above, has a brilliant appearance.
If, in the above washing agent, instead of the pyrazine mentioned, 0.08 parts of 3.5-bis-methylarnino-pyrazine- 2.6-dicarboxylic acid methylamide or 0.005 parts of 3.5- bis-methylamino-pyrazine-2-carboxylic acid phenylarnide- 6-carboxylic acid methylamide are used, then a brightening effect is also obtained.
Example 10 0.1 parts of 3.S-bis-methylamino-pyrazine-Z-carboxylic acid phenylamide-6-carboxylic acid methylamide are added to 100 parts of washing agent consisting of 30% of a condensation product of oleic acid and methyl taurine, 65% sodium sulphate and 5% water.
Nylon fabric Washed at 50 in a washing liquor containing 5 parts per litre of the washing agent described has a much more white appearance than fabric washed without the addition of brightening agent.
. Acetate silk fabric washed under the same conditions with a washing agent of the same composition but containing 0.15 parts of 3.5-bis-ethylamino-pyraZine-2.6-dicarboxylic acid ethylamide instead of the pyrazine named, also has a beautiful white appearance.
Also a Washing agent consisting of the condensation product of oleic acid and taurine can be used instead of that described. t
Example 11 0.075 parts of 3-ethylamino-S-methylarnino-pyrazine- 2.6-dicar.boxylic acid ethylamide are incorporated into 100 parts of washing agent consisting of 25% of a sulphonated condensation product of p-methoxyphenyl diguanide and oleic acid (1-p-methoXyphenyl-2imino-4- amino-6oleyl-1.3.5-triazine sulphonic acid), 70% sodium sulphate and 5% water.
Nylon fabric washed at 50 in a washing liquor (liquor ratio 1:30) which contains 5 parts per litre of the Washing agent described above, has a brilliant appearance.
Wool fabric washed under the same conditions with the above washing agent but containing 0.15 parts of 3.5-bisethylamino-pyrazine-2.6-dicarboxylic acid ethylamide instead of the pyrazine named, also has a very beautiful White appearance.
A beautiful brightening effect on acetate silk is obtained if, in the washing agent described above, 0.075 parts of 3.S-bis-methylamino-pyrazine-2-carboxylic acid phenylamide-6-carboxylic acid ethylamide are used instead of the pyrazine mentioned.
The present application is a division of co-pending application, Ser. No. 737,215, filed May 23, 1958.
What we claim is:
1. A composition of matter of improved appearance in daylight consisting essentially of an uncoloured carrier selected from the group consisting of synthetic polypeptides, natural poly-peptides, vinyl polymers and cellulose acetates, containing from 0.001 to 0.5% by weight, of the 1 composition, of a 3.S-diamino-pyraZine-Z.G-dicarboxylic acid amide of the formula:
wherein R R and R each is a member selected from the group consisting of lower alkyl and phenyl substituted methyl radicals and X is a member selected from the group consisting of primary amino, secondary amino, tertiary amino and ureido groups.
2. A composition of matter of improved appearance in daylight consisting of wool and from 0.001 to 0.5% by Weight, of the composition, of a 3.5-diamino-pyrazine-2.6- dicarboxylic acid amide of the formula:
wherein R R and R each is a member selected from the group consisting of lower alkyl and phenyl substituted methyl radicals and X is a member selected from the group consisting of primary amino, secondary amino, tertiary amino and ureido groups.
3. A composition of matter of improved appearance in daylight consisting of nylon and from 0.001 to 0.5 by weight, of the composition, of a 3.5-diamino-pyraZine-2,6- dicarboxylic acid amide of the formula:
wherein R R and R each is a member selected from I the group consisting of lower alkyl and phenyl substituted methyl radicals and X is a member selected from the group consisting of primary amino, secondary amino, tertiary amino and ureido groups.
4. A composition of matter of improved appearance in daylight consisting of cellulose acetate and from 0.001 to 0.5% by weight, of the composition, of a 3.5-diaminopyrazine-Z.6-dicarboxylic acid amide of the formula:
wherein R R and R each is a member selected from the group consisting of lower alkyl and phenyl substituted methyl radicals and X is a member selected from the group consisting of primary amino, secondary amino, tertiary amino and ureido groups.
6. A composition of matter of improved appearance in daylight consisting of polystyrene and from 0.001 to 0.5 by weight, of the composition, of a 3.5-diamino-pyrazine- 2.6-dicarb0xylic acid amide of the formula:
wherein R R and R each is a member selected from the group consisting of lower alkyl and phenyl substituted methyl radicals and X is a member selected from the group consisting of primary amino, secondary amino, tertiary amino and ureido groups.
7. A composition of matter of improved appearance in daylight consisting of polyethylene and from 0.001 to 0.5% by weight, of the composition, of a 3.5-diaminopyrazine-Z.6-dicarboxylic acid amide of the formula:
wherein R R and R each is a member selected from the group consisting of lower alkyl and phenyl substituted methyl radicals and X is a member selected from the group consisting of primary amino, secondary amino, tertiary amino and ureido groups.
References Cited in the file of this patent UNITED STATES PATENTS 2,581,889 Timmis Jan. 8, 1952 2,972,611 Zweidler et al Feb. 21, 1961 3,063,994 Adams et al Nov. 13, 1962 OTHER REFERENCES Raybin: Chemical Abstracts, vol. 39 (1945) 44333.
Taylor: Chemical Abstracts, vol. 49 (1955) 6966 and 6967