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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2777Generated: October 26, 2026

6-Chlorobenzo[b]thiophene-2-sulfonyl chloride → 6-Chlorobenzo[b]thiophene-2-sulfonic acid [1-(5-cyano-2-hydroxy-benzyl)-2-oxo-pyrrolidin-3-(S)-yl]-amide

https://huagongshe.com/reaction/2777

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Chlorobenzo[b]thiophene-2-sulfonyl chlorideHCID 15158641—
Reactant3-[(3-Amino-2-oxo-pyrrolidin-1-yl)-methyl]-4-hydroxy-benzonitrile hydrochlorideHCID 19350910—
Product6-Chlorobenzo[b]thiophene-2-sulfonic acid [1-(5-cyano-2-hydroxy-benzyl)-2-oxo-pyrrolidin-3-(S)-yl]-amideHCID 54521297—

Reaction Steps

The title compound is prepared from 3-[(3-amino-2-oxo-pyrrolidin-1-yl)-methyl]-4-hydroxy-benzonitrile hydrochloride as described in EXAMPLE 17, Part G substituting 6-chlorobenzo[b]thiophene-2-sulfonyl chloride in place of 4,6-dichlorobenzo[b]thiophene-2-sulfonyl chloride. The crude product is triturated with Et2O to give the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05731315
Source datasetuspto-grants-1998_03
ORD IDord-5319433aef944914adab5a67046697cc
Source noteuspto-grants-1998_03