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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2073231Generated: October 30, 2026

Acetic Acid → HCID 19858110, compound

https://huagongshe.com/reaction/2073231

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant3-(Aminosulfonyl)-4-chlorobenzoyl chlorideHCID 3017979—
ReactantHCID 19858102HCID 19858102—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
ProductHCID 19858110HCID 1985811055.2%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04916149
Source datasetuspto-grants-1990_04
ORD IDord-4a31ca967056488ead3123f9a4faef8e
Source noteuspto-grants-1990_04