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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1630666Generated: October 31, 2026

Tris(furan-2-yl)phosphane → methyl 1-(3-chloropyridin-2-yl)-3-{[6-(trifluoromethyl)pyridin-3-yl]methyl}-1H-pyrazole-5-carboxylate

https://huagongshe.com/reaction/1630666

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTris(furan-2-yl)phosphaneHCID 521585—
Reactant5-Tributylstannyl-2-trifluoromethylpyridineHCID 17959541—
Reactantmethyl 3-(bromomethyl)-1-(3-chloropyridin-2-yl)-1H-pyrazole-5-carboxylateHCID 66659984—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Productmethyl 1-(3-chloropyridin-2-yl)-3-{[6-(trifluoromethyl)pyridin-3-yl]methyl}-1H-pyrazole-5-carboxylateHCID 66587532—

Reaction Steps

Under argon, 0.8 g (2.36 mmol) of methyl 3-(bromomethyl)-1-(3-chloropyridin-2-yl)-1H-pyrazole-5-carboxylate, 1.18 g (2.60 mmol) of 5-(tributylstannyl)-2-(trifluoromethyl)pyridine, 0.11 g (0.47 mmol) of tri-2-furylphosphine and 0.07 g (0.07 mmol) of tri(dibenzylideneacetone)dipalladium were stirred in NMP at 100° C. for 2 h. The solvent was distilled off under reduced pressure, and the residue was taken up in 80 ml of ethyl acetate and stirred vigorously with 70 ml of saturated potassium fluoride solution for 60 min. The organic phase was separated off, washed once with saturated sodium chloride solution, dried over sodium sulphate and concentrated using a rotary evaporator. The desired product was obtained by chromatographic purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08791139B2
Source datasetuspto-grants-2014_07
ORD IDord-db99f7fc5bbb46798e3a25066bedb5f1
Source noteuspto-grants-2014_07