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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1278189Generated: November 3, 2026

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

https://huagongshe.com/reaction/1278189

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 numberUS04281003
Source datasetuspto-grants-1981_07
ORD IDord-77d0287908d94600903deb953a7eed4c
Source noteuspto-grants-1981_07