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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1357903Generated: November 1, 2026

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

https://huagongshe.com/reaction/1357903

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 numberUS06593346B2
Source datasetuspto-grants-2003_07
ORD IDord-5428918efbe041efa28d99971b373f6e
Source noteuspto-grants-2003_07