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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1470552Generated: October 30, 2026

Potassium Carbonate → HCID 86691194, compound

https://huagongshe.com/reaction/1470552

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3-(Trifluoromethyl)phenylboronic acidHCID 2734388—
Reactanttert-butyl ((1R,2S)-2-(6-bromopyridin-3-yl)cyclopropyl)carbamateHCID 86691195—
SolventAcetonitrile--water (1/1)HCID 18373917—
ProductHCID 86691194HCID 8669119458.3%

Reaction Steps

A solution of tert-butyl (trans)-2-(6-bromopyridin-3-yl)cyclopropylcarbamate (Intermediate J[a2]) (100 mg, 0.32 mmol), potassium carbonate (132 mg, 0.96 mmol) and 3-trifluoromethylbenzeneboronic acid (72 mg, 0.38 mmol) in CH3CN:H2O (4:1) (10 mL) was degassed for 30 mins, added tetrakis triphenylphosphine palladium (37 mg, 0.032 mmol), degassed for 10 mins and heated the reaction mixture at reflux temperature for 2 h. After completion, the reaction mixture was poured in ice water (100 mL), extracted with ethyl acetate (5×40 mL). The combined extract were washed with water (70 mL), brine (70 mL), dried over anhydrous Na2SO4, filtered and evaporated. The crude residue was purified by column chromatography (SiO2), by using EtOAc:Petroleum ether (1:9) to get tert-butyl (trans)-2-(6-(3-(trifluoromethyl)phenyl)pyridin-3-yl)cyclopropylcarbamate (70 mg, 58.3%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006449B2
Source datasetuspto-grants-2015_04
ORD IDord-6aaa35cb040d496684cfc9ab09e26116
Source noteuspto-grants-2015_04