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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 734653Generated: October 25, 2026

2,3-Dichlorobenzene-1-sulfonyl chloride → 2-Acetylamino-4-[4-(2,3-dichlorobenzenesulphonylamino)phenyl]-1H-pyrrole-3-carboxamide

https://huagongshe.com/reaction/734653

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-Dichlorobenzene-1-sulfonyl chlorideHCID 2734222—
Reactant2-acetylamino-4-(4-aminophenyl)-1H-pyrrole-3-carboxamideHCID 69061860—
SolventPyridineHCID 1049—
Product2-Acetylamino-4-[4-(2,3-dichlorobenzenesulphonylamino)phenyl]-1H-pyrrole-3-carboxamideHCID 57845566—

Reaction Steps

A suspension of 70 mg (0.271 mmol) of 2-acetylamino-4-(4-aminophenyl)-1H-pyrrole-3-carboxamide and 70 mg (0.285 mmol) of 2,3-dichlorobenzene-sulphonyl chloride in 1.5 cm3 of pyridine is stirred at room temperature for 24 hours and then the reaction medium is evaporated to dryness under reduced pressure. The crude product is purified by flash chromatography [eluent; dichloromethane/methanol (97/3 by volume)]. After concentrating under reduced pressure the fractions containing the expected product, 22 mg of 2-acetylamino-4-[4-(2,3-dichlorobenzenesulphonylamino)phenyl]-1H-pyrrole-3-carboxamide are obtained in the form of a beige solid melting at 265° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07592365B2
Source datasetuspto-grants-2009_09
ORD IDord-4eb77725a27b4e64aeb9a0b37e5f4096
Source noteuspto-grants-2009_09