Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2267505Generated: November 1, 2026

Triethylamine → 5-bromo-3-[1-(ethenylsulfonyl)-4-piperidinyl]-1H-indole-7-carboxamide

https://huagongshe.com/reaction/2267505

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthanesulfonylchloride, 2-chloro-HCID 15385—
Reactant5-bromo-3-(4-piperidinyl)-1H-indole-7-carboxamideHCID 11324722—
SolventDichloromethaneHCID 6344—
Product5-bromo-3-[1-(ethenylsulfonyl)-4-piperidinyl]-1H-indole-7-carboxamideHCID 5900333575%

Reaction Steps

To a solution of 5-bromo-3-(4-piperidinyl)-1H-indole-7-carboxamide (500 mg, 1.3 mmol) in methylene chloride at room temperature, triethylamine (0.44 mL, 3.2 mmol) and 2-chloroethylsulfonyl chloride (0.168 mL, 1.6 mmol) were added. The reaction mixture was stirred for 30 min. Removed the solvent, the residue was purified by combiflash to give the title compound (150 mg, 75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858796B2
Source datasetuspto-grants-2010_12
ORD IDord-3edf6b06962f496fb11934866b28b78b
Source noteuspto-grants-2010_12