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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1947656Generated: October 30, 2026

Cesium carbonate → Tert-butyl 1'-[2-(trifluoromethyl)pyrimidin-4-yl]-4,4'-bipiperidine-1-carboxylate

https://huagongshe.com/reaction/1947656

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant4,4'-Bipiperidine, 1-boc protectedHCID 11747599—
Reactant4-Bromo-2-(trifluoromethyl)pyrimidineHCID 53302344—
SolventEthyl AcetateHCID 8857—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductTert-butyl 1'-[2-(trifluoromethyl)pyrimidin-4-yl]-4,4'-bipiperidine-1-carboxylateHCID 59178917—

Reaction Conditions

Temperature70 °C

Reaction Steps

The tert-butyl 4,4′-bipiperidine-1-carboxylate (28.5 mg, 0.11 mmol) and cesium carbonate (106 mg, 0.32 mmol) were stirred in NMP (0.5 ml) and the 4-bromo-2-(trifluoromethyl)pyrimidine (12 mg, 0.053 mmol) was added. The mixture was heated at 70° C. for 2 h. The reaction was cooled down to r.t. and diluted with ethyl acetate (5 mL) and was washed with water 2 mL (×1) and brine 2 mL (×1). The organic phase was dried over magnesium sulfate, filtered, and concentrated on rotavapor. The crude material was purified by preparative TLC with 30% acetone: hexane to yield the titled compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399485B2
Source datasetuspto-grants-2013_03
ORD IDord-f44710e0fdbe4ca2997ba5e289987449
Source noteuspto-grants-2013_03