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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1486728Generated: October 30, 2026

Cyclopentylamine → 1-[3-(4-Chloro-benzoylamino)-benzyl]-piperidine-4-carboxylic acid cyclopentylamide

https://huagongshe.com/reaction/1486728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopentylamineHCID 2906—
ReactantN,N-diethyl-m-toluamideHCID 4284—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantDiisopropylethylamineHCID 81531—
ReactantHOAtHCID 181649—
Reactant[3-(4-Chloro-benzoylamino)-benzyl]-piperidine-4-carboxylic acidHCID 86706549—
SolventDimethylformamideHCID 6228—
Product1-[3-(4-Chloro-benzoylamino)-benzyl]-piperidine-4-carboxylic acid cyclopentylamideHCID 72703638—

Reaction Conditions

Temperature50 °C

Reaction Steps

1-Cyclopentylamine (10.7 mg, 0.124 mmol) is added to a solution of [3-(4-chloro-benzoylamino)-benzyl]-piperidine-4-carboxylic acid (35.4 mg, 0.095 mmol) in DMF (0.5 mL). The resulting solution is treated with a solution of HOAT (15.5 mg, 0.114 mmol) in DMF (0.5 mL) followed by si-DCC (200 mg, 0.95 mmol/g, 0.19 mmol), and DIPEA (0.033 mL, 0.19 mmol). The mixture is stirred at 50° C. overnight. PI-DETA (7.99 mmol/g, 0.3 mmol, 37 mg) is added to the solution in order to scavenge the acid, PI-NCO (2.24 mmol/g, 0.3 mmol, 130 mg) is added to scavenge the amine in excess and the mixture is stirred for 1 h. The resin is filtered and washed with a mixture of MeOH/DCM 1:1, (4×1 mL). The resulting solution is evaporated under HV. The title compound is obtained by prep. HPLC F as a colourless powder: LC-MS A: tR=1.21 min; [M+H]+=440.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09428456B2
Source datasetuspto-grants-2016_08
ORD IDord-53983610fcaf4968b472859bc7f491ce
Source noteuspto-grants-2016_08