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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 609736Generated: October 25, 2026

Triethylamine → 5-(cyclohex-1-en-1-yl)-3-(2-pyrrolidinylethyl)-1H-indole

https://huagongshe.com/reaction/609736

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant5-(1-hydroxycyclohex-1-yl)-3-(2-pyrrolidinylethyl)-1H-indoleHCID 69948706—
SolventDichloromethaneHCID 6344—
ProductAmmoniaHCID 2225%
Product5-(cyclohex-1-en-1-yl)-3-(2-pyrrolidinylethyl)-1H-indoleHCID 6994899492.6%

Reaction Steps

Methanesulfonyl chloride (0.042 mL, 0.54 mmol) was added to a solution of 5-(1-hydroxycyclohex-1-yl)-3-(2-pyrrolidinylethyl)-1H-indole (Example 13a, 50.6 mg, 0.16 mmol) and triethylamine (0.15 mL, 1.06 mmol) in dichloromethane (2.5 mL) at 0° C. The reaction was allowed to warm slowly to room temperature and stirring was continued overnight. The reaction mixture was diluted with dichloromethane (100 mL) and washed sequentially with water and brine, dried over sodium sulfate and the solvent was removed in vacuo. Flash chromatography (silica, 5-8% 2M methanolic ammonia in dichloromethane) yielded 5-(cyclohex-1-en-1-yl)-3-(2-pyrrolidinylethyl)-1H-indole (21.8 mg, 46%); HRMS-FAB+ for C20H26N2 :calculated MH+ :295.21744; found MH+ :295.21953.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05998438
Source datasetuspto-grants-1999_12
ORD IDord-1ef81c29f2d24351ac8876be0312f581
Source noteuspto-grants-1999_12