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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 736414Generated: October 30, 2026

Methyl 1-[(4-{[(tert-butoxycarbonyl)amino]methyl}piperidine-1-yl)methyl]cyclopentanecarboxylate → Methyl 1-{[4-(aminomethyl)piperidin-1-yl]methyl}cyclopentanecarboxylate

https://huagongshe.com/reaction/736414

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 1-[(4-{[(tert-butoxycarbonyl)amino]methyl}piperidine-1-yl)methyl]cyclopentanecarboxylateHCID 67232469—
SolventDichloromethaneHCID 6344—
SolventTrifluoroacetic acidHCID 6422—
ProductMethyl 1-{[4-(aminomethyl)piperidin-1-yl]methyl}cyclopentanecarboxylateHCID 67232206100%

Reaction Steps

A solution of methyl 1-[(4-{[(tert-butoxycarbonyl)amino]methyl}piperidine-1-yl)methyl]cyclopentanecarboxylate (1.16 g, 3.27 mmol, Step2) in CH2Cl2 (25 mL) and trifluoroacetic acid (5 mL) was stirred at room temperature for 1.5 h. The reaction mixture was then concentrated and basified with sat. NaHCO3 aq. (100 mL), extracted with CHCl3 (100 mL) for five times. The combined extract was dried and concentrated to give 0.831 g (100%) of title compound as yellow syrup.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07595329B2
Source datasetuspto-grants-2009_09
ORD IDord-6cf6402b7d914d99b4956daa63b0e016
Source noteuspto-grants-2009_09