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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 717881Generated: November 4, 2026

Diisopropylethylamine → Tert-butyl 4-{[6-chloro-2-(trifluoromethyl)pyrimidin-4-yl]amino}piperidine-1-carboxylate

https://huagongshe.com/reaction/717881

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Amino-1-Boc-piperidineHCID 1268291—
Reactant4,6-Dichloro-2-trifluoromethylpyrimidineHCID 15713197—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 4-{[6-chloro-2-(trifluoromethyl)pyrimidin-4-yl]amino}piperidine-1-carboxylateHCID 86706861—

Reaction Steps

tert-Butyl 4-aminopiperidine-1-carboxylate (1.4 g, 7.1 mmol, Aldrich) was dissolved in methylene chloride (10. mL) and to this solution was added N,N-diisopropylethylamine (2.5 mL, 14 mmol) and 4,6-dichloro-2-(trifluoromethyl)pyrimidine (1.7 g, 7.8 mmol, Synchem). The reaction was stirred overnight. The mixture was diluted with water and the product was extracted with EtOAc. The organic layer was washed twice with water, once with brine, dried over sodium sulfate, filtered and concentrated to afford product which was used without further purification in Step 2. LCMS (M+H)+: 381.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193733B2
Source datasetuspto-grants-2015_11
ORD IDord-52d7c2cab18c4fe4b12dea61ef15a833
Source noteuspto-grants-2015_11