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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1508951Generated: October 30, 2026

2-(3-Chlorophenyl)-5,6,7,8-tetrahydroquinazolin-4-ol → 4-Chloro-2-(3-chlorophenyl)-5,6,7,8-tetrahydroquinazoline

https://huagongshe.com/reaction/1508951

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(3-Chlorophenyl)-5,6,7,8-tetrahydroquinazolin-4-olHCID 135830943—
ReactantHCID 178479711HCID 178479711—
Product4-Chloro-2-(3-chlorophenyl)-5,6,7,8-tetrahydroquinazolineHCID 2214343588.5%

Reaction Conditions

Temperature100 °C

Reaction Steps

Phosphorus(V) oxychloride (17.6 g, 114.7 mmol) was slowly added to 2-(3-chlorophenyl)-5,6,7,8-tetrahydroquinazolin-4(3H)-one (2.2 g, 8.5 mmol) at 0° C. The reaction mixture was warmed to 100° C. and held at that temperature for 2 h. After this time, the mixture was cooled, quenched with saturated sodium hydroxide, and extracted with ethyl acetate. The combined organic layer was dried over anhydrous sodium sulfate, filtered, and the filtrate was concentrated. The residue was purified by column chromatography (silica, hexanes/dichloromethane) to afford the title compound (2.1 g, 23%) as a white solid. MW=279.16. 1H NMR (CDCl3, 300 MHz) δ 8.43-8.37 (m, 1H), 8.32-8.24 (m, 1H), 7.49-7.33 (m, 2H), 3.03-2.87 (m, 2H), 2.86-2.70 (m, 2H), 1.98-1.83 (m, 4H); APCI MS m/z 279 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221843B2
Source datasetuspto-grants-2015_12
ORD IDord-2e16016657874eceadde636b35b41cc8
Source noteuspto-grants-2015_12