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US3933847A
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Method relating to manufacture of coumarin derivatives
Assignee: Sumitomo Chemical Co Ltd
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Filing: 1973-12-19
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Granted: 1976-01-20
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Expires: 1993-12-19
Abstract
Abstract A coumarin dye of the formula (Ia), WHEREIN R1 is hydrogen, chlorine or C1-C2 alkyl, R2 and R3 are hydrogen or C1 -C4 alkyl, or a quarternary salt thereof having the formula (Ib), WHEREIN R1, R2 and R3 are as defined above, R4 is C1-C2 alkyl or benzyl, and X<-> is an anion, is prepared by an improved method, which comprises reacting a diamine of the formula, WHEREIN R1 is as defined above, with a compound of the formula, X - CH2 - Y wherein X and Y are the same or different and are carboxyl, carbamoyl, alkoxycarbonyl or cyano, in 10 to 70 % sulfuric acid to prepare an imidazolyl acetic acid of the formula, WHEREIN R1 is as defined above, and then reacting the imidazolyl acetic acid with a compound of the formula, WHEREIN R2 and R3 are as defined above, to obtain the dye (Ia), or further reacting the resulting dye (Ia) with an alkylating agent to obtain the dye (Ib).
Inventors
- 👤 Masaaki Ohkawa
- 👤 Koichi Ishii
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-29 07:39
CPC Classifications
C; C09; C09B; C09B57/00; C09B57/02
Claims Analysis
Total Claims: 11
Claim 1
Independent Claim
223 words
A method for preparing a coumarin dye of the formula (Ia), ##SPC19## wherein R 1 is a hydrogen or chlorine atom, or a C 1 - C 2 alkyl group, R 2 and R 3 are each a hydrogen atom or a C 1 - C 4 alkyl group, or a quarternary salt of the dye (Ia) of the formula (Ib), ##SPC20## wherein R 1 , R 2 and R 3 are as defined above, R 4 is a C 1 - C 2 alkyl or benzyl group and X - is an anion, which comprises reacting a diamine of the formula (II), ##SPC21## wherein R 1 is as defined above, with a compound of the formula (III), X -- CH.sub.2 -- Y (III) wherein X and Y may be the same or different, and are each a carboxyl, carbamoyl, alkoxycarbonyl or cyano group, in a 10 to 70% sulfuric acid to prepare a benzimidazolyl acetic acid of the formula (IV), ##SPC22## wherein R 1 is as defined above, and then reacting the compound thus obtained with a hydroxybenzaldehyde of the formula (V), ##SPC23## wherein R 2 and R 3 are as defined above, to obtain the dye of the formula (Ia), or reacting the resulting dye of the formula (Ia) with an alkylating agent to obtain the dye of the formula (Ib).
Claim 2
Independent Claim
223 words
A method for preparing a coumarin dye of the formula (Ia), ##SPC19## wherein R 1 is a hydrogen or chlorine atom, or a C 1 - C 2 alkyl group, R 2 and R 3 are each a hydrogen atom or a C 1 - C 4 alkyl group, or a quarternary salt of the dye (Ia) of the formula (Ib), ##SPC20## wherein R 1 , R 2 and R 3 are as defined above, R 4 is a C 1 - C 2 alkyl or benzyl group and X - is an anion, which comprises reacting a diamine of the formula (II), ##SPC21## wherein R 1 is as defined above, with a compound of the formula (III), X -- CH.sub.2 -- Y (III) wherein X and Y may be the same or different, and are each a carboxyl, carbamoyl, alkoxycarbonyl or cyano group, in a 10 to 70% sulfuric acid to prepare a benzimidazolyl acetic acid of the formula (IV), ##SPC22## wherein R 1 is as defined above, and then reacting the compound thus obtained with a hydroxybenzaldehyde of the formula (V), ##SPC23## wherein R 2 and R 3 are as defined above, to obtain the dye of the formula (Ia), or reacting the resulting dye of the formula (Ia) with an alkylating agent to obtain the dye of the formula (Ib).
Claim 3
Dependent Claim
30 words
The method according to claim 1, wherein the diamine of the formula (II) is a member selected from the group consisting of o-phenylenediamine, 4- or 5-methyl-o-phenylenediamine and 4- or 5-chloro-o-phenylenediamine.
Claim 4
Dependent Claim
37 words
The method according to claim 1, wherein the compound of the formula (III) is a member selected from the group consisting of malonic acid, malonic acid diesters, cyanoacetic acid, cyanoacetic acid esters, cyanoacetamide, N-alkylcyanoacetamides, allylamide and dicyanomethane.
Claim 5
Dependent Claim
28 words
The method according to claim 1, wherein the hydroxybenzaldehyde of the formula (V) is a member selected from the group consisting of 2-hydroxy-4-dimethylaminobenzaldehyde, 2-hydroxy-4-aminobenzaldehyde, 2-hydroxy-4-diethylaminobenzaldehyde, 2-hydroxy-4-ethylaminobenzaldehyde and 2-hydroxy-4-dibutylaminobenzaldehyde.
Claim 6
Dependent Claim
32 words
The method according to claim 1, wherein the compound of the formula (III) is used in an amount of at least 1 mole per mole of the diamine of the formula (II).
Claim 7
Dependent Claim
29 words
The method according to claim 1, wherein the hydroxybenzaldehyde of the formula (V) is used in an almost equimolar amount to the benzimidazolyl acetic acid of the formula (IV).
Claim 8
Dependent Claim
39 words
The method according to claim 1, wherein the reaction between the diamine of the formula (II) and the compound (III) is carried out at a temperature of about 90° to about 120°C. for about 3 to about 15 hours.
Claim 9
Dependent Claim
44 words
The method according to claim 1, wherein the reaction between the benzimidazolyl acetic acid of the formula (IV) and the hydroxybenzaldehyde of the formula (V) is carried out at a temperature of about 50° to about 100°C. for about 30 to about 180 minutes.
Claim 10
Dependent Claim
38 words
The method according to claim 1, wherein the alkylating agent is a member selected from one group consisting of dimethyl sulfate, diethyl sulfate, benzyl chloride. methyl bromide, ethyl bromide, methyl benzenesulfonate, ethyl benzenesulfonate, methyl p-toluenesulfonate and ethyl p-toluenesulfonate.
Claim 11
Dependent Claim
26 words
The method according to claim 1, wherein the alkylation is carried out in an inert organic solvent at a temperature of about 80° to about 130°C.
References Cited (Backward Citations)
USPTO Annuity & Maintenance Windows
| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
|---|---|---|---|---|---|
| 3.5 Years (Year 4) | 1979-01-19 | 1979-07-21 | 1980-01-20 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1983-01-19 | 1983-07-21 | 1984-01-20 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1987-01-19 | 1987-07-21 | 1988-01-20 | $7700.00 | Window Closed / Lapsed |