Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 3-(Aminosulfonyl)-4-chlorobenzoyl chloride | HCID 3017979 | — |
| Reactant | HCID 19858102 | HCID 19858102 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 19858110 | HCID 19858110 | 55.2% |
Reaction Steps
2.54 g of 4-chloro-3-sulfamoylbenzoyl chloride were added in little portions to the solution of 2.2 g of 1-amino-5-methoxycarbonylbenzimidazole-2-thione in 8 ml of dimethylformamide and 1.4 ml of triethylamine while stirring. The reaction mixture was set aside overnight, then the pH value was adjusted to 5 by acetic acid and it was diluted with 100 ml of water. The separated gum slowly disaggregated to a powder which was filtered by suction, washed with water and dried at 80° C. The crude product obtained was boiled with 10 ml of glacial acetic acid for 30 minutes, then poured into 50 ml of water. The separated gum disaggregated to a powder by stirring. The precipitate was filtered by suction, washed with water and dried at 80° C. to give 2.4 g (54.5%) of 1-(4'-chloro-3'-sulfamoylbenzoyl)amino-5-methoxycarbonylbenzimidazole-2-thione, as a beige powder, m.p.: 258°-261° C. (with decomposition) after recrystallization from a mixture of dimethylformamide and water (1:2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04916149 |
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| Source dataset | uspto-grants-1990_04 |
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| ORD ID | ord-4a31ca967056488ead3123f9a4faef8e |
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| Source note | uspto-grants-1990_04 |
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