참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hexane | HCID 8058 | — |
| 반응물 | Thionyl Chloride | HCID 24386 | — |
| 반응물 | 5-Benzyloxy-2-fluoro-4-methylaniline | HCID 21991068 | — |
| 반응물 | 7-Acetoxy-6-methoxy-3,4-dihydroquinazolin-4-one | HCID 135697905 | — |
| 촉매 | Dimethylformamide | HCID 6228 | — |
| 용매 | Isopropanol | HCID 3776 | — |
| 생성물 | 7-Acetoxy4-(5-benzyloxy-2-fluoro-4-methylanilino)-6-methoxyquinazoline | HCID 21260312 | 43% |
반응 단계
A mixture of 7-acetoxy-6-methoxy-3,4-dihydroquinazolin-4-one (1.69 g, 7.2 mmol), thionyl chloride (50 ml) and DMF (3 drops) was heated at reflux for 2 hours. The excess thionyl chloride was removed by evaporation and the residue azeotroped with toluene. The residue was partitioned between methylene chloride and saturated aqueous sodium hydrogen carbonate solution. The organic phase was separated, dried (MgSO4) and the solvent removed by evaporation. 5-Benzyloxy-2-fluoro-4-methylaniline (1.8 g, 7.8 mmol) in isopropanol (50 ml) was added to the residue and the mixture heated at reflux for 2 hours. The mixture was allowed to cool, hexane added and the precipitated product collected by filtration to give 7-acetoxy-4-(5-benzyloxy-2-fluoro-4-methylanilino)-6-methoxyquinazoline (1.34 g, 43%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06184225B2 |
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| 출처 데이터셋 | uspto-grants-2001_02 |
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| ORD ID | ord-ebb58f8a97c24a4e87a477c597871eff |
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| 출처 메모 | uspto-grants-2001_02 |
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