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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1676089Generated: October 29, 2026

Benzenesulfonyl chloride → HCID 58653660, compound

https://huagongshe.com/reaction/1676089

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 58653671HCID 58653671—
SolventDichloromethaneHCID 6344—
ProductHCID 58653660HCID 58653660—

Reaction Steps

To a solution of methyl 3-(5-amino-1H-benzimidazol-1-yl)-3-(1,1′-biphenyl)-4-ylpropanoate (15 mg, 40 μmol) in dichloromethane (500 μL) was added benzenesulfonyl chloride (6.0 μL, 47 μmol) and N,N-diisopropylethylamine (8.0 μL, 46 μmol). The solution was stirred at room temperature for 48 hours, and was then evaporated in vacuo. The residue was purified by flash column chromatography on silica gel, eluting with a mixture of dichloromethane and methanol (96:4), to afford the title compound, [LCMS (Method A, Mobile Phase I) RT=5.50 min, MH+ 513].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003806B2
Source datasetuspto-grants-2011_08
ORD IDord-d5d2490db9ec43f29aed1c800c881cc7
Source noteuspto-grants-2011_08