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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 461187Generated: October 30, 2026

Triethylamine → 4-[4-Chloro-3-(2,4-dimethoxybenzylsulfamoyl)-phenyl]-3-methyl-2-methylimino-1,3-thiazolidine-4-ol-hydrochloride

https://huagongshe.com/reaction/461187

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2,4-DimethoxybenzylamineHCID 597250—
Reactant4-Chloro-3-chlorosulfonylphenyl-3-methyl-2-methylimino-1,3-thiazolidine-4-ol-hydrobromideHCID 22760489—
SolventWaterHCID 962—
Product4-[4-Chloro-3-(2,4-dimethoxybenzylsulfamoyl)-phenyl]-3-methyl-2-methylimino-1,3-thiazolidine-4-ol-hydrochlorideHCID 22760419—

Reaction Steps

8.8 g of 4-(4-chloro-3-chlorosulfonylphenyl)-3-methyl-2-methylimino-1,3-thiazolidine-4-ol-hydrobromide were reacted as prescribed in Example 76 with 5 g of triethyl amine and 3.5 g of 2,4-dimethoxybenzyl amine and worked up. After treating with water, the amorphous 4-[4-chloro-3-(2,4-di-methoxybenzylsulfamoyl)-phenyl]-3-methyl-2-methylimino-1,3-thiazolidine-4-ol was extracted with 70 ml of ethyl acetate, dried over sodium sulfate and the solvent was acidified with ethanolic hydrochloric acid (15%). The amorphous precipitate end product was crystallized under isopropanol. Melting point: 163° C (decomposition).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04061761
Source datasetuspto-grants-1977_12
ORD IDord-e0f110ab932d4ec8b2faec9f46b1793e
Source noteuspto-grants-1977_12