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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1393601Generated: November 1, 2026

Water → 4-[[(4-Chlorophenyl)sulfonyl][1,2-diphenyl-1H-benzimidazol-5-yl]amino]butanoic acid methyl ester

https://huagongshe.com/reaction/1393601

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
ReactantMethyl 4-bromobutyrateHCID 107604—
Reactant4-Chloro-N-(1,2-diphenyl-1H-benzimidazol-5-yl)benzenesulfonamideHCID 21938028—
SolventDimethylformamideHCID 6228—
Product4-[[(4-Chlorophenyl)sulfonyl][1,2-diphenyl-1H-benzimidazol-5-yl]amino]butanoic acid methyl esterHCID 67364031—

Reaction Conditions

Temperature20 °C

Reaction Steps

100 mg of 4-chloro-N-(1,2-diphenyl-1H-benzimidazol-5-yl)benzenesulfonamide was suspended in 0.5 ml of N,N-dimethylformamide, mixed with 6 mg of sodium hydride and stirred for 30 minutes at 20° C. 56 mg of 4-bromobutyric acid methyl ester was added, it was allowed to stir for 15 hours, mixed with water, extracted three times with ethyl acetate, the extracts were dried on sodium sulfate, concentrated by evaporation in a vacuum, and the residue was digested with diisopropyl ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07345075B2
Source datasetuspto-grants-2008_03
ORD IDord-9414f8de2ee44cc49b3d9dc96fa4293b
Source noteuspto-grants-2008_03