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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2091267Generated: November 1, 2026

Benzenesulfonyl chloride → HCID 66778378, compound

https://huagongshe.com/reaction/2091267

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 66778821HCID 66778821—
SolventDimethylacetamideHCID 31374—
ProductHCID 66778378HCID 6677837896%

Reaction Steps

To a solution (10 mL) of ethyl 3-{[(4-{[(5-amino-3-methyl-1-benzofuran-2-yl)(cyclohexyl)methyl]amino}phenyl)carbonyl](methyl)amino}-propanoate (254 mg) synthesized in Example A110(5) in N,N-dimethylacetamide was added benzenesulfonyl chloride (99 μL), and the mixture was stirred overnight at room temperature. Saturated aqueous ammonium chloride solution was added to quench the reaction, and the reaction mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (30-70% ethyl acetate/hexane) to give the title object compound (312 mg, 96%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436043B2
Source datasetuspto-grants-2013_05
ORD IDord-c86b2a1949bb488c86d86ee7eec94e28
Source noteuspto-grants-2013_05