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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1278186Generated: October 27, 2026

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

https://huagongshe.com/reaction/1278186

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-5-(trifluoromethyl)pyridineHCID 735862—
Reactant2,6-Difluorobenzamidocarboxylic acid, 4-nitrophenyl esterHCID 57286081—
Product1-(2,6-Difluorobenzoyl)-3-(5-trifluoromethyl-2-pyridinyl)ureaHCID 12800603—

Reaction Steps

A portion of 5-trifluoromethyl-2-aminopyridine is dissolved in an inert organic solvent, and to the solution is added a portion of 2,6-difluorobenzamidocarboxylic acid, 4-nitrophenyl ester. The reaction mixture is stirred at elevated temperature for a period of time, after which the reaction mixture is evaporated to dryness under vacuum, and the product named in the heading above, identical to the product of Example 1, is isolated by recrystallization.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04281003
Source datasetuspto-grants-1981_07
ORD IDord-b3145ff5191d4589bee3f52e36913bba
Source noteuspto-grants-1981_07