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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 278216Generated: October 31, 2026

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

https://huagongshe.com/reaction/278216

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 numberUS06358979B1
Source datasetuspto-grants-2002_03
ORD IDord-c5456e180a604dc788c1a6e4508f6470
Source noteuspto-grants-2002_03