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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2230135Generated: October 30, 2026

5-Chloro-3-methylbenzo(b)thiophene-2-sulfonyl chloride → HCID 18180112, compound

https://huagongshe.com/reaction/2230135

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Chloro-3-methylbenzo(b)thiophene-2-sulfonyl chlorideHCID 2735756—
Reactant3-Methoxy-4-(4-methylpiperazin-1-yl)anilineHCID 11844761—
SolventDichloromethaneHCID 6344—
ProductHCID 18180112HCID 1818011234%

Reaction Steps

A solution of 3-methoxy-4-(4-methylpiperazin-1-yl)phenylamine (D35) (50 mg, 0.23 mmol) and 5-chloro-3-methylbenzo[b]thiophene-2-sulfonyl chloride (64 mg, 0.23 mmol) in dichloromethane (2 ml) was allowed to stand at room temperature overnight. The reaction mixture was diluted with dichloromethane and washed with potassium carbonate (aq), which was back-extracted with further dichloromethane. The combined organic phases were dried (Na2SO4) and evaporated under reduced pressure to give a crude product, which was purified by chromatography on silica gel, eluting with methanol and dichloromethane. This gave the title compound (E128) as an off-white solid (36 mg, 34%) MH+=466.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06423717B1
Source datasetuspto-grants-2002_07
ORD IDord-125e53b526214c88b7b74850ac0275bb
Source noteuspto-grants-2002_07