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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 429149Generated: October 29, 2026

Pyridine → 6-Chloro-1-(4-methoxy-3-piperazin-1-ylbenzenesulfonyl)-5-methyl-2,3-dihydro-1H-indole hydrochloride

https://huagongshe.com/reaction/429149

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantHCID 11178065HCID 11178065—
Reactant6-Chloro-5-methyl-2,3-dihydro-1H-indoleHCID 22186080—
SolventDichloromethaneHCID 6344—
Product6-Chloro-1-(4-methoxy-3-piperazin-1-ylbenzenesulfonyl)-5-methyl-2,3-dihydro-1H-indole hydrochlorideHCID 18354549110.3%

Reaction Steps

Pyridine (0.28 ml) was added to a stirred solution of 6-chloro-5-methyl-2,3-dihydro-1H-indole (WO-9501976) (0.116 g) and 3-(4-trichloroacetylpiperazin-1-yl)-4-methoxybenzenesulfonyl chloride (D4) (300 mg) in dichioromethane (4 ml) at room temperature. After 18 h the solution was washed with 1M hydrochloric acid (5 ml), water (5 ml), dried (MgSO4) and concentrated to an oil. The oil was dissolved in 1,4-dioxan (13 ml) and a 0.15 M potassium hydroxide solution (6.5 ml) was added. The solution was stirred at room temperature for 4 h then concentrated to remove the organic solvent, diluted with water (10 ml) and the solution extracted with dichloromethane (20 ml). The organic phase was dried (Na2SO4), acidified with 1M ethereal hydrogen chloride (2 ml), concentrated to a solid and stirred with acetone to afford the title compound (0.175 g, 55%). MH+ 422/424.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06316450B1
Source datasetuspto-grants-2001_11
ORD IDord-8e0f5063581d4fe9b011a3ff69a13f43
Source noteuspto-grants-2001_11