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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2303623Generated: November 2, 2026

2-Chloropyrimidine → tert-butyl 4-(pyrimidin-2-ylamino)piperidine-1-carboxylate

https://huagongshe.com/reaction/2303623

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChloropyrimidineHCID 74404—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Amino-1-Boc-piperidineHCID 1268291—
SolventIsopropanolHCID 3776—
SolventDichloromethaneHCID 6344—
Producttert-butyl 4-(pyrimidin-2-ylamino)piperidine-1-carboxylateHCID 276394936.7%

Reaction Steps

4-Amino-1-t-butoxycarbonylpiperidine from Step A, (1.9 g, 9.5 mmol), 2-chloropyrimidine (1.1 g, 9.5 mmol) and DIPEA (3.3 mL, 19 mmol) were combined in isopropanol (10 mL) and the mixture was refluxed for 24 h. The mixture was cooled, diluted with methylene chloride (100 mL) and washed with water and brine. The organic phase was dried over sodium sulfate and concentrated. FC (60 g silica, 1/1 hexanes/ethyl acetate) afforded the title compound (0.97 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06432981B1
Source datasetuspto-grants-2002_08
ORD IDord-00d96024b9d54f309e563f5e9ca44053
Source noteuspto-grants-2002_08