Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2188466Generated: November 1, 2026

Phosphorus oxychloride → 4-Methoxy-5-phenyl-2,6-bis-(4-pyridyl)-pyrimidine

https://huagongshe.com/reaction/2188466

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantSodium MethoxideHCID 10942334—
Reactant2-Chloro-5-(4-fluorophenyl)-4-(4-pyridyl)-pyrimidineHCID 23000365—
Reactant4-Chloro-5-phenyl-2,6-bis-(4-pyridyl)-pyrimidineHCID 23000417—
Reactant5-phenyl-2,6-bis-(4-pyridyl)-4(3H)-pyrimidinoneHCID 135703015—
SolventMethanolHCID 887—
Product4-Methoxy-5-phenyl-2,6-bis-(4-pyridyl)-pyrimidineHCID 23000521—

Reaction Steps

A mixture of 5-phenyl-2,6-bis-(4-pyridyl)-4(3H)-pyrimidinone (360 mg, 1.10 mmol) and phosphorus oxychloride (2 ml) was heated at reflux for 1.5 h. Work-up was done as described for the preparation of 2-chloro-5-(4-fluorophenyl)-4-(4-pyridyl)-pyrimidine. To a solution of the crude 4-chloro-5-phenyl-2,6-bis-(4-pyridyl)-pyrimidine (250 mg, 0.73 mmol) in methanol (5 ml) was added methanolic 0.5 N sodium methoxide (1.45 ml, 0.73 mmol) and it was heated at reflux for 1 h. After evaporation, the resultant material was partitioned between ethyl acetate and water. The organic solution was washed with water, dried and evaporated. Chromatography of the crude product on a column of silica gel (ethyl acetate) provided the title compound. MS (m/z): 341.2 (M+H)+; C21H16N4O requir. 340.4 1H-NMR (CDCl3) 8.82, 8.54, 8.40 (3m, each 2H, Pyrid.), 7.40-7.18, (m, 7H, Ph. Pyrid.), 4.15 (s, 3H, CH3O).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06410729B1
Source datasetuspto-grants-2002_06
ORD IDord-41fa5ff37ac34a58a98a15c9ce25de1c
Source noteuspto-grants-2002_06