Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1765241Generated: October 31, 2026

4-(Chloromethyl)benzoyl chloride → 4-chloromethyl-N-[4-methyl-3-(2-pyridin-4-yl-6-(trifluoromethyl)pyrimidin-4-ylamino)-phenyl]benzamide

https://huagongshe.com/reaction/1765241

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Chloromethyl)benzoyl chlorideHCID 70136—
Reactant4-(5-Amino-2-methylanilino)-2-(4-pyridinyl)-6-(trifluoromethyl)pyrimidineHCID 22732458—
Product4-chloromethyl-N-[4-methyl-3-(2-pyridin-4-yl-6-(trifluoromethyl)pyrimidin-4-ylamino)-phenyl]benzamideHCID 22732364—

Reaction Steps

The title compound was prepared from a mixture of 4-(5-amino-2-methylanilino)-2-(4-pyridinyl)-6-(trifluoromethyl)pyrimidine (80 mg, 0.232 mmol) and 4-chloromethylbenzoyl chloride (53 mg, 0.278 mmol) similar to Example 139 and isolated as a yellow solid (55 mg, 48%). 1H NMR (CDCl3): 8.75 (dd, J=1.8, 4.8 Hz, 2H), 8.29 (dd, J=1.8, 4.8 Hz, 2H), 8.02 (s, 1H), 7.96 (s, 1H), 7.88 (d, J=8.4 Hz, 2H), 7.51 (d, J=8.4 Hz, 2H), 7.37 (dd, J=1.8, 7.5 Hz, 1H), 7.32 (d, J=7.5 Hz, 1H), 7.12 (s, 1H), 6.75 (s, 1H), 4.63 (s, 2H), 2.28 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07226927B2
Source datasetuspto-grants-2007_06
ORD IDord-e84603100503401c949a9900a171fb8f
Source noteuspto-grants-2007_06