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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1758936Generated: November 3, 2026

2-Amino-5-(trifluoromethyl)pyridine → 1-(2-Chloro-6-fluorobenzoyl)-3-(5-trifluoromethyl-2-pyridinyl)urea

https://huagongshe.com/reaction/1758936

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-5-(trifluoromethyl)pyridineHCID 735862—
Reactant2-Chloro-6-fluorobenzamidocarboxylic acid, 4-nitrophenyl esterHCID 57040980—
Product1-(2-Chloro-6-fluorobenzoyl)-3-(5-trifluoromethyl-2-pyridinyl)ureaHCID 20533138—

Reaction Steps

A solution is made in an inert organic solvent of 2-chloro-6-fluorobenzamidocarboxylic acid, 4-nitrophenyl ester, and 5-trifluoromethyl-2-aminopyridine. The temperature of the reaction mixture is raised, and the mixture is stirred for a period of time. The mixture is then evaporated under vacuum, and the product named in the heading above, identical to the product of Example 4, is isolated and purified by recrystallization.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04338321
Source datasetuspto-grants-1982_07
ORD IDord-fe51f3d1bab841e5a29b9c9038b3bfe0
Source noteuspto-grants-1982_07