Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 645976Generated: October 26, 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/645976

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, Step 2) 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 numberUS07705020B2
Source datasetuspto-grants-2010_04
ORD IDord-1859f03b69ce4bf5bb5e4320782f2240
Source noteuspto-grants-2010_04