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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 730219Generated: October 30, 2026

HCID 43151386, compound → HCID 86605044, compound

https://huagongshe.com/reaction/730219

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 43151386HCID 43151386—
ReactantBenzo[b]thiophene-2-sulfonic acid (2-aminophenyl)amideHCID 86240018—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductHCID 86605044HCID 86605044119.4%

Reaction Steps

To a solution of benzo[b]thiophene-2-sulfonic acid (2-amino-phenyl)-amide (1 mmol, prepared as in Example 1) in DCM (2 mL) and pyridine (2 mL), 5-methanesulfonyl-2-methoxybenzenesulfonyl chloride (1.1 mmol) was added at RT and the reaction mixture was then allowed to stir at RT overnight. The reaction mixture was then diluted with DCM (10 mL). The organic phase was washed with 10% aqueous HCl (10 mL), water (10 mL) and brine (10 mL). The organic phase was dried over anhydrous sodium sulfate and concentrated under vacuum. The residue obtained was purified by flash column chromatography eluting with DCM/EtOAc to obtain 330 mg of benzo[b]thiophene-2-sulfonic acid [2-(4-methanesulfonyl-2-methoxy-benzenesulfonylamino)phenyl]-amide. LC: Tr 1.06 min; MS: 553.8 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582673B2
Source datasetuspto-grants-2009_09
ORD IDord-bfee53af254e47c393714f1e6efdc86f
Source noteuspto-grants-2009_09