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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1016140Generated: October 31, 2026

Cyclopentanecarbonyl chloride → HCID 57889875, compound

https://huagongshe.com/reaction/1016140

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopentanecarbonyl chlorideHCID 78284—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 86614926HCID 86614926—
SolventDichloromethaneHCID 6344—
ProductHCID 57889875HCID 57889875—

Reaction Steps

Benzyl (R)-4-amino-5-((S)-4-(4-chlorophenyl)-4-hydroxy-3,3-dimethylpiperidin-1-yl)-5-oxopentylcarbamate hydrochloride (50.5 mg, 0.096 mmol) was dissolved in dichloromethane (0.5 mL) and added cyclopentane carbonylchloride (14 μL, 0.12 mmol) followed by DIPEA (42 μL, 0.24 mmol). The solution was stirred for 2 h, concentrated, and partitioned between EtOAc (2 mL) and aq NaHCO3 (0.5 mL). The EtOAc layer was separated, dried over magnesium sulfate, and concentrated to give benzyl (R)-5-((S)-4-(4-chlorophenyl)-4-hydroxy-3,3-dimethylpiperidin-1-yl)-4-(cyclopentanecarboxamido)-5-oxopentylcarbamate which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07985861B2
Source datasetuspto-grants-2011_07
ORD IDord-0537026f1a424f1c862fd3b4042ea05c
Source noteuspto-grants-2011_07