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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946664Generated: October 23, 2026

Triethylamine → 6-chloro-N-(4-hydroxy-2-methylphenyl)pyrimidine-4-carboxamide

https://huagongshe.com/en/reaction/1946664

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Amino-m-cresolHCID 17819—
Reactant6-Chloropyrimidine-4-carbonyl chlorideHCID 18422098—
Reactant6-chloro-N-(4-hydroxyphenyl)pyrimidine-4-carboxamideHCID 59446876—
SolventDichloromethaneHCID 6344—
Product6-chloro-N-(4-hydroxy-2-methylphenyl)pyrimidine-4-carboxamideHCID 59447105—

Reaction Steps

A cooled (0° C.) solution of 4-amino-m-cresol (Fluka, 4.17 g, 33.9 mmol) and triethylamine (23.6 mL, 0.170 mol) in dry dichloromethane (100 mL) was treated with 6-chloropyrimidine-4-carbonyl chloride, obtained as described above for Intermediate 7, step 1 (6.0 g, 34 mmol) and the resulting mixture was stirred at room temperature for 12 hours. The reaction mixture was concentrated in vacuo, diluted with water and extracted with EtOAc. The combined organic layers were dried on magnesium sulfate and evaporated in vacuo. The crude product was purified by column chromatography (silica) using as eluent petroleum ether/EtOAc to afford the title compound as yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399448B2
Source datasetuspto-grants-2013_03
ORD IDord-293e601e98894baca4aea202277ee4ff
Source noteuspto-grants-2013_03