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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2091951Generated: November 3, 2026

Triethylamine → 4'-(4-Chloro-5-(trifluoromethyl)pyrimidin-2-ylamino)-5'-methoxy-N,2'-dimethylbiphenyl-4-carboxamide

https://huagongshe.com/reaction/2091951

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2,4-Dichloro-5-(trifluoromethyl)pyrimidineHCID 2782774—
Reactant4'-Amino-5'-methoxy-N,2'-dimethylbiphenyl-4-carboxamideHCID 59586791—
CatalystZincchlorideHCID 3007855—
Solvent1,2-DichloroethaneHCID 11—
Solventtert-ButanolHCID 6386—
Product4'-(4-Chloro-5-(trifluoromethyl)pyrimidin-2-ylamino)-5'-methoxy-N,2'-dimethylbiphenyl-4-carboxamideHCID 86647793—

Reaction Steps

To the mixture of 2,4-dichloro-5-(trifluoromethyl)pyrimidine (100 mg, 0.46 mmol) in 0.5 mL of DCE and 0.5 mL of t-BuOH is added zinc chloride (1.0 M in ether, 0.46 mL, 0.46 mmol), and stirred 30 min. 4′-amino-5′-methoxy-N,2′-dimethylbiphenyl-4-carboxamide (111 mg, 0.414 mmol) and triethylamine (46 mg, 0.46 mmol) are added sequentially, and the reaction is stirred at room temperature overnight. The precipitate is filtered, washed by MeOH, and dried in vacuo to afford 4′-(4-Chloro-5-(trifluoromethyl)pyrimidin-2-ylamino)-5′-methoxy-N,2′-dimethylbiphenyl-4-carboxamide as a white solid; ESMS m/z 451.1 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08440681B2
Source datasetuspto-grants-2013_05
ORD IDord-c0ed4d1ae9114672a198ece0ddd6b8c6
Source noteuspto-grants-2013_05