HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1271217Generated: October 27, 2026
Phosphorus oxychloride → 7-Bromo-4-chloro-2-methylquinazoline
https://huagongshe.com/reaction/1271217
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 7-Bromo-2-methylquinazolin-4(3H)-one | HCID 135804503 | — |
| Solvent | N,N-Dimethylaniline | HCID 949 | — |
| Product | 7-Bromo-4-chloro-2-methylquinazoline | HCID 22247819 | 60.2% |
Reaction Steps
A suspension of 0.45 g (1.87 mmol) of 7-bromo-2-methyl-3H-quinazolin-4-one in 0.48 ml N,N-dimethylaniline was treated with 1.41 ml (15.4 mmol) phosphorous oxychloride and heated at 60° C. for 2 h. The reaction mixture was evaporated in vacuo and the residue taken up in 20 ml water, neutralized with 10 ml saturated aqueous sodium bicarbonate and twice extracted with 25 ml dichloromethane. The organic layer is washed with 25 ml water, 25 ml brine, dried over magnesium sulfate and evaporated in vacuo. The residue is purified by chromatography on silica gel with heptane/ethylacetate (2:1) to give 0.29 g (59%) of 7-bromo-4-chloro-2-methyl-quinazoline as an orange solid. Mp. >82° C. EI mass spectrum, m/e: 258 (M calculated for C9H6BrClN2: 258).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07205309B2 |
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| Source dataset | uspto-grants-2007_04 |
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| ORD ID | ord-e9a5f005bd4f4cc18c9c6347c15f37f2 |
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| Source note | uspto-grants-2007_04 |
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