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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1278176Generated: November 1, 2026

2-Amino-5-(trifluoromethyl)pyridine → 1-(2,6-Difluorobenzoyl)-3-(5-trifluoromethyl-2-pyridinyl)urea

https://huagongshe.com/reaction/1278176

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-5-(trifluoromethyl)pyridineHCID 735862—
Reactant2,6-Difluorobenzoyl isocyanateHCID 2733369—
SolventAcetonitrileHCID 6342—
Product1-(2,6-Difluorobenzoyl)-3-(5-trifluoromethyl-2-pyridinyl)ureaHCID 12800603—

Reaction Steps

An 0.7 g. portion of 5-trifluoromethyl-2-aminopyridine was dissolved in 20 ml. of acetonitrile, and to the solution was added 0.85 g. of 2,6-difluorobenzoyl isocyanate under a nitrogen blanket at ambient temperature. A precipitate formed immediately. The mixture was stirred for 3 hours, and was then filtered and the solids were washed with acetonitrile. The solids were dried under vacuum to obtain 1.0 g. of the product named above, m.p. 215°-220° C. Elemental analysis gave the following results:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04281003
Source datasetuspto-grants-1981_07
ORD IDord-fc3aa789986944659c9237b58e0cdf8d
Source noteuspto-grants-1981_07