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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946722Generated: October 27, 2026

O-Toluidine → N-(4-hydroxyphenyl)-6-(o-tolylamino)pyrimidine-4-carboxamide

https://huagongshe.com/reaction/1946722

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-ToluidineHCID 7242—
ReactantDiisopropylethylamineHCID 81531—
Reactant6-chloro-N-(4-hydroxyphenyl)pyrimidine-4-carboxamideHCID 59446876—
Reactant6-chloro-N-(4-hydroxy-2-methylphenyl)pyrimidine-4-carboxamideHCID 59447105—
SolventEthanolHCID 702—
ProductN-(4-hydroxyphenyl)-6-(o-tolylamino)pyrimidine-4-carboxamideHCID 25182757—

Reaction Conditions

Temperature160 °C

Reaction Steps

A solution of 6-chloro-N-(4-hydroxy-2-methylphenyl)pyrimidine-4-carboxamide, Intermediate 7 (50.0 mg; 0.20 mmol) in ethanol (3 mL) was treated with N-ethyldiisopropylamine (69 μl; 0.4 mmol) and o-toluidine (Fluka, 21.5 μl; 0.20 mmol). The reaction mixture was heated at 160° C. for 3 hours under microwave irradiation. The solvents were removed in vacuo, EtOAc was added and the organic phase was washed with a citric acid solution, dried over magnesium sulfate then evaporated in vacuo. The crude product was purified by column chromatography (silica), eluting with cyclohexane containing an increasing amount of EtOAc. The title compound was obtained as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399448B2
Source datasetuspto-grants-2013_03
ORD IDord-9fea9813494c424b91095330d685074a
Source noteuspto-grants-2013_03