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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2225173Generated: November 1, 2026

Phosphorus oxychloride → HCID 21075094, compound

https://huagongshe.com/reaction/2225173

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantHCID 178489278HCID 178489278—
ProductHCID 21075094HCID 21075094—

Reaction Steps

Preparation D6, Step 3. A suspension of 6-(2-methoxyphenyl)quinazolin-4-ol (250 mg, 0.99 mmol) in POCl3 (10 mL) was heated at reflux for 1 h, during which time a clear solution was observed. The mixture was cooled to room temperature, concentrated in-vacuo, then concentrated from methylene chloride (3×100 mL) to remove any remaining POCl3. The residue was partitioned between ethyl acetate (25 mL) and saturated NaHCO3 (30 mL), and the mixture was stirred until gas evolution ceased (10 min). The layers were separated, the organic phase was washed with saturated NaHCO3, water, and brine, dried over sodium sulfate, and concentrated in-vacuo. The residue was purified over silica gel, eluting with 1:3 ethyl acetate/heptane, to yield 217 mg of 4-chloro-6-(2-methoxyphenyl)quinazoline as a white solid. 1H NMR (500 MHz, CDCl3) δ ppm 9.03 (s, 1 H), 8.36 (s, 1 H), 8.19 (d, J=7.15 Hz, 1 H), 8.10 (d, J=8.80 Hz, 1 H), 7.42 (m, 2 H), 7.10 (t, J=7.42 Hz, 1 H), 7.04 (d, J=8.25 Hz, 1 H), 3.86 (m, 3 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07378409B2
Source datasetuspto-grants-2008_05
ORD IDord-f234f55c25064b70b8c1ae00a49a544f
Source noteuspto-grants-2008_05