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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877692Generated: October 31, 2026

Boron trifluoride → 1-(5-Fluoropyrimidin-2-yl)cyclopropanamine

https://huagongshe.com/reaction/1877692

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluorideHCID 6356—
ReactantTetrahydrofuranHCID 8028—
Reactant5-Fluoropyrimidine-2-carbonitrileHCID 44181867—
ReactantHCID 178418443HCID 178418443—
CatalystTitanium isopropoxideHCID 11026—
SolventWaterHCID 962—
Product1-(5-Fluoropyrimidin-2-yl)cyclopropanamineHCID 67291362—

Reaction Steps

To a solution of 5-fluoropyrimidine-2-carbonitrile (200 mg, 1.6 mmol, 1 eq) in a dry THF under an argon atmosphere was added titanium isopropoxide (0.55 ml, 1.9 mmol, 1.2 eq) at ambient temperature and the reaction mixture was stirred for 15 min. Ethyl magnesium bromide (1M solution) in THF (4 ml, 4.0 mmol, 2.5 eq) was added via syringe slowly at ambient temperature. Then the reaction mixture was stirred for an hour. BF3.EtO (0.34 ml, 2.4 mmol, 1.5 eq) was added slowly through syringe to the mixture at 0° C. The mixture was allowed to attain ambient temperature and stirred for another one hour. 10 ml of water was added to the reaction mixture which was then filtered through Celite and the bed washed with water and ethyl acetate. The filtrate was basified with 10% NaOH solution (pH=9) then extracted with DCM and washed with brine solution, dried over sodium sulphate and concentrated to give the crude product which was taken for coupling reaction without further purification. Yield: 125 mg (crude).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309558B2
Source datasetuspto-grants-2012_11
ORD IDord-326a8c8d26544f86904dd07ff4d1f786
Source noteuspto-grants-2012_11