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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50656Generated: October 26, 2026

Diisopropylethylamine → [1-(4-Chloro-phenyl)-cyclopentyl]-(3-hydroxymethyl-piperidin-1-yl)-methanone

https://huagongshe.com/reaction/50656

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1-(4-Chlorophenyl)cyclopentanecarboxylic acidHCID 97447—
ReactantPiperidin-3-ylmethanolHCID 107308—
ReactantPyBroPHCID 2733179—
SolventDichloromethaneHCID 6344—
Product[1-(4-Chloro-phenyl)-cyclopentyl]-(3-hydroxymethyl-piperidin-1-yl)-methanoneHCID 22335026156.9%

Reaction Steps

A solution of piperdin-3-yl methanol (0.342 g, 2.97 mmol), 1-(4-chloro-phenyl)-cyclopentylcarboxylic acid (1.0 g, 4.45 mmol), diisopropylethyl amine (1.9, 15.00 mmol) in dichloromethane (7 mL) was stirred at room temperature. PyBroP (2.07 g, 4.45 mmol) was added and the reaction mixture continued stirring at room temperature. After 12 h the reaction mixture was quenched with 10% KOH. The aqueous layer was extracted with ethyl acetate. The combined organic layers were dried over sodium sulfate and concentrated to yield a crude oil. The crude material was purified using silica gel chromatography (95:5 hexane:ethyl acetate) to yield the desired compound (1.50 g). C18H24ClNO2, LRMS (m/z)=322 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06713479B2
Source datasetuspto-grants-2004_03
ORD IDord-f01119f38d2b4a158dbe36d70edafa10
Source noteuspto-grants-2004_03