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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1693005Generated: October 27, 2026

Phosphorus oxychloride → 4-Chloro-2-(2-methoxy-phenyl)-7-methyl-quinazoline

https://huagongshe.com/reaction/1693005

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 136105219HCID 136105219—
SolventTolueneHCID 1140—
Product4-Chloro-2-(2-methoxy-phenyl)-7-methyl-quinazolineHCID 59212857—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a mechanically stirred suspension of 2-(2-methoxyphenyl)-7-methyl-3H-quinazolin-4-one (100 g, 0.37 mol) in 1 L toluene was added diisopropyl ethylamine (100 mL), followed by phosphorus oxychloride (69 g, 0.45 mol). The reaction was then heated to 80° C. for 4 h. The reaction mixture was distilled under reduced pressure to remove toluene, and the resulting residue was dissolved in 2.2 L CH2Cl2. Ice water was added, and the pH was adjusted to 8-9 with saturated aqueous sodium bicarbonate solution while maintaining the temperature below 20° C. The resulting organic layer was separated and the aqueous solution extracted with CH2Cl2, then the combined the organic layers were dried over sodium sulfate and distilled under reduced pressure. The crude product was dissolved 2:1 CH2Cl2/hexane, and the solution was passed through silica gel (2.5 kg, 60-120 mesh), followed by washing the silica bed with 2:1 CH2Cl2/hexane until the product eluted. The pure fractions were collected and combined, and the solvent was removed under reduced pressure. Hexane (500 mL) was added, and the mixture was stirred and filtered to give 4-chloro-2-(2-methoxy-phenyl)-7-methyl-quinazoline as a white to off-white solid (77 g, 72%). mp 161-164° C. 1H NMR (CDCl3) δ 2.6 (s, 3H), 3.9 (s, 3H), 6.9-7.2 (m, 2H), 7.4-7.6 (m, 2H), 7.7-8 (d, 2H), 8.2 (d, 1H) ppm; M/z (obs., [m+H]+)=285.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158637B2
Source datasetuspto-grants-2012_04
ORD IDord-2d2a6bfa96ac4f869c3402f8e489d301
Source noteuspto-grants-2012_04