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US4450274A
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Preparation of ethambutol-diisoniazide methane sulfonic acid salt
Assignee: Korea Advanced Institute of Science and Technology
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Filing: 1982-06-10
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Granted: 1984-05-22
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Expires: 2002-06-10
Abstract
Abstract This invention pertains to a new process for preparing an ethambutol-sulfonic acid derivative which is widely used as an antituberculosis agent. In the known process, there are many defects which include: side reactions, impurities, low yield, high cost production inefficiency and pollution hazard. For the purpose of preparing an ethambutol-sulfonic acid derivative of a higher purity and higher yield than the known process, ethambutol or its hydrogen chloride salt is reacted with chloromethane sulfonic acid or its sodium salt in the lower alcoholic solvent such as methanol, ethanol, propanol, or isopropanol, at a temperature between room temperature and boiling point of the solvent, for about an hour, to produce ethambutol-chloromethane-sulfonate which is then reacted with isoniazid to produce the ethambutol-sulfonic acid derivative of the present invention.
Inventors
- 👤 Sang-Woo Park
Bibliographic Details
Application Number
—
Jurisdiction
US
Data Source
google_patents
Last Synchronized
2026-10-27 11:05
CPC Classifications
C; C07; C07D; C07D213/00; C07D213/02; C07D213/04; C07D213/60; C07D213/78; C07D213/86; C07D213/81; C07D213/82; A; A61; A61P; A61P31/00; A61P31/04; A61P31/06
Claims Analysis
Total Claims: 12
Claim 1
Independent Claim
17 words
A process for preparing an d(+) 2,2-(ethylene diimino) dibutanol-diisoniazide-methane-sulfonate comprising reacting isoniazid with ethylene diimino dibutanol-chloro-methane sulfonate.
Claim 2
Dependent Claim
17 words
A process for preparing an d(+) 2,2-(ethylene diimino) dibutanol-diisoniazide-methane-sulfonate comprising reacting isoniazid with ethylene diimino dibutanol-chloro-methane sulfonate.
Claim 3
Dependent Claim
45 words
A process for preparing d(+) 2,2-(ethylene diimino) dibutanol-diisoniazide-methane-sulfonate according to claim 1, wherein the ethylene diimino dibutanol-chloro-methane sulfonate reactant is produced by reacting a chloro-methane sulfonic acid with a compound selected from the group consisting of ethylene diimino dibutanol and the hydrogen chloride salt thereof.
Claim 4
Dependent Claim
31 words
A process for preparing d(+) 2,2-(ethylene diimino) dibutanol-diisoniazide-methane sulfonate according to claim 2, wherein the chloro-methane-sulfonic acid is of the general formula Cl--CH.sub.2 --SO.sub.3 --R wherein R represents H or Na.
Claim 5
Dependent Claim
20 words
A process for preparing d(+) 2,2-(ethylenediimino) dibutanol-diisoniazide-methane sulfonate according to claim 1, wherein the reaction time is about one hour.
Claim 6
Dependent Claim
26 words
A process for preparing d(+) 2,2-(ethylene diimino) dibutanol-diisoniazide-methane sulfonate according to claim 1, wherein the reaction is carried out in the presence of alkaline activated alumina.
Claim 7
Dependent Claim
62 words
A process for preparing d(+) 2,2-(ethylene diimino) dibutanol-diisoniazide-methane sulfonate according to claim 1, wherein the reaction of the ethylene diimino dibutanol or its hydrogen chloride salt with the chloro-methane sulfonic acid is carried out in a solvent comprising a lower aliphatic alcohol containing not more than four carbon atoms, and wherein the reaction with isoniazid then is carried out without any separation.
Claim 8
Dependent Claim
43 words
A process for preparing d(+) 2,2-(ethylene diimino) dibutanol-diisoniazide-methane sulfonate according to claim 6, wherein the reaction of the ethylene diimino dibutanol-chloro-methane sulfonate with isoniazid is carried out at a temperature of between about room temperature and about the boiling temperature of the solvent.
Claim 9
Dependent Claim
47 words
A process for preparing d(+) 2,2-(ethylene diimino) dibutanol-diisoniazide-methane sulfonate according to claim 6, wherein the reaction of the ethylene diimino dibutanol hydrogen chloride salt with the chloro-methane sulfonic acid or its sodium salt is carried out at a temperature of between about 100° and about 110° C.
Claim 10
Dependent Claim
31 words
A process for preparing d(+) 2,2-(ethylene diimino) dibutanol-diisoniazide-methane sulfonate according to claim 7, wherein the reaction between isoniazid and ethylene diimino dibutanol-chloro-methane sulfonate proceeds for between about 20 and 30 minutes.
Claim 11
Dependent Claim
71 words
A process for preparing d(+) 2,2'-(ethylene diimino) dibutanol-diisoniazid-methane sulfonate comprising the steps of (a) reacting in alcohol under reflux conditions an ethylene diimino dibutanol of the formula ##STR4## with a compound of the formula Cl--CH.sub.2 --SO.sub.3 --R wherein R=Na (b) removing by filtration sodium chloride formed; (c) adding isoniazid to the product of step (b); and (d) heating the reaction mixture at 100°-110° C. for between about 20 and 30 minutes.
Claim 12
Dependent Claim
71 words
A process for preparing d(+) 2,2'-(ethylene diimino) dibutanol-diisoniazid-methane sulfonate comprising the steps of (a) reacting in alcohol under reflux conditions an ethylene diimino dibutanol of the formula ##STR4## with a compound of the formula Cl--CH.sub.2 --SO.sub.3 --R wherein R=Na (b) removing by filtration sodium chloride formed; (c) adding isoniazid to the product of step (b); and (d) heating the reaction mixture at 100°-110° C. for between about 20 and 30 minutes.
References Cited (Backward Citations)
US3718655A
Cited
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| Annuity Stage | Window Opens | Payment Deadline | Surcharge Period Until | Estimated Fee | Status |
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| 3.5 Years (Year 4) | 1987-05-22 | 1987-11-21 | 1988-05-22 | $2000.00 | Window Closed / Lapsed |
| 7.5 Years (Year 8) | 1991-05-22 | 1991-11-21 | 1992-05-22 | $3760.00 | Window Closed / Lapsed |
| 11.5 Years (Year 12) | 1995-05-22 | 1995-11-21 | 1996-05-22 | $7700.00 | Window Closed / Lapsed |