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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1358960Generated: October 30, 2026

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

https://huagongshe.com/reaction/1358960

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 numberUS06599904B2
Source datasetuspto-grants-2003_07
ORD IDord-e63ee4a5cb2449c883e15be37e900b42
Source noteuspto-grants-2003_07