HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443215Generated: October 28, 2026
Phosphorus pentachloride → 2-Methylquinazolin-5-amine
https://huagongshe.com/reaction/1443215
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphorus pentachloride | HCID 24819 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 136342146 | HCID 136342146 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Phosphorus oxychloride | HCID 24813 | — |
| Product | 2-Methylquinazolin-5-amine | HCID 17985058 | 5.4% |
Reaction Steps
12.7 g (62 mmol) of 2-methyl-5-nitro-3H-quinazolin-4-one (M. T. Bogert, V. J. Chambers J. Org Chem. 1905, 649-658) and 37.5 g of phosphorus pentachloride are refluxed in 75 ml of phosphoryl chloride over 20 hours. After cooling, it is poured into saturated NaHCO3 solution and extracted with ethyl acetate. The organic phase is dried, and the solvent is removed. 14 g of 4-chloro-2-methyl-5-nitroquinazoline, of which 4.5 g (20.2 mmol) in 225 ml of ethyl acetate and 22.5 ml of triethylamine are dissolved, is obtained. 2 g of palladium on carbon is added, and it is stirred while being cooled with ice for 4 hours under a hydrogen atmosphere at normal pressure. Catalyst is removed from the solution by means of filtration through Celite, whereby it is rewashed with 200 ml of ethanol and concentrated by evaporation. After chromatography on silica gel with ethyl acetate-ethanol (0-10%), 530 mg of the product is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07659297B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-f3958abb3e6f455db09c1b214b028f9f |
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| Source note | uspto-grants-2010_02 |
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