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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 459467Generated: October 26, 2026

Triethylamine → (+/-)-cis-N-(5-Chloro-1-phenylsulfonylindole-2-sulfonyl)-1,2-cyclopentanediamine

https://huagongshe.com/reaction/459467

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactantcis-Cyclopentane-1,2-diamineHCID 11412654—
Reactant5-Chloro-1-phenylsulfonylindole-2-sulfonyl chlorideHCID 23513737—
Reactant5-chloro-1-phenyl-3-sulfonyl-2H-indole-2-sulfonyl chlorideHCID 86593056—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product(+/-)-cis-N-(5-Chloro-1-phenylsulfonylindole-2-sulfonyl)-1,2-cyclopentanediamineHCID 18442845407.2%

Reaction Steps

cis-1,2-Cyclopentanediamine (WO98/30574) (348 mg) was dissolved in dichloromethane (10 ml), and to the solution triethylamine (1 ml) and 5-chloro-1-phenyl-sulfonylindole-2-sulfonyl chloride (390 mg) were added at 0° C. with stirring. After 15 minutes and 1 hour, 5-chloro-1-phenylsulfonylindole-2-sulfonyl chloride (156 mg) was additionally added. After stirring for 15 minutes, 5-chloro-1-phenylsulfonylindole-2-sulfonyl chloride (78 mg) was further added, and the mixture was stirred at room temperature for 2 hours. Water was added to the reaction mixture to separate an organic layer. The resultant organic layer was washed with a saturated solution of sodium hydrogencarbonate and dried over anhydrous sodium sulfate. The residue was purified by flash column chromatography on silica gel (chloroform:methanol=23:2) to obtain the title compound (739 mg) as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07192968B2
Source datasetuspto-grants-2007_03
ORD IDord-fa9b32c2f4414841805c0ee2d9939cea
Source noteuspto-grants-2007_03