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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 347619Generated: October 30, 2026

5-Chloro-3-methylbenzo(b)thiophene-2-sulfonyl chloride → HCID 10182243, compound

https://huagongshe.com/reaction/347619

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Chloro-3-methylbenzo(b)thiophene-2-sulfonyl chlorideHCID 2735756—
Reactant3-(2-DIMETHYLAMINO-ETHYL)-1H-INDOL-5-YLAMINEHCID 11820211—
SolventPyridineHCID 1049—
ProductHCID 10182243HCID 1018224382%

Reaction Steps

To a solution of 3.05 g (15 mMol) of 5-amino-3-(2-dimethylaminoethyl)-1H-indol in 100 ml of pyridine is added dropwise at ambient temperature a solution of 4.21 g (15 mMol) of 5-chloro-3-methyl-benzo[b]thiophene-2-sulphonyl chloride in 20 ml of pyridine. The reaction mixture is stirred at ambient temperature for 20 hours. It is then evaporated to dryness, slightly alkalinised with diluted ammonia and dissolved in ethyl acetate. The organic phase is washed with water and a saturated solution of sodium bicarbonate, it is separated and dried with anhydrous sodium sulphate. The organic solution is evaporated to dryness and the resulting solid is repeatedly washed with ethyl ether, to yield 5.5 g (82%) of N-[3-(2-dimethylaminoethyl)-1H-indol-5-yl]-5-chloro-3-methyl-benzo[b]thiophene-2-sulphonamide as a solid with m.p.=226–227° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176200B2
Source datasetuspto-grants-2007_02
ORD IDord-3d68f9ae31be455ebfea0c0b7d10e94c
Source noteuspto-grants-2007_02