참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | Formamidine | HCID 68047 | — |
| 반응물 | 4-Fluoroanthranilic acid | HCID 2724967 | — |
| 반응물 | 4-Chloro-7-fluoro-6-nitroquinazoline | HCID 10609358 | — |
| 용매 | 2-Methoxyethanol | HCID 8019 | — |
| 생성물 | 7-Fluoroquinazolin-4(3H)-one | HCID 135398496 | — |
반응 단계
4-Chloro-7-fluoro-6-nitroquinazoline (7) can be prepared by methods similar to those described in J. Med. Chem. 1996, 39, 918-928. Generally, 2-amino-4-fluoro-benzoic acid (1) can be reacted with formamidine (2) and acetic acid (3) in the presence of 2-methoxyethanol to provide 7-Fluoro-3H-quinazolin-4-one (4). The 7-fluoro-3H-quinazolin-4-one (4) can then be nitrated to 7-fluoro-6-nitro-3H-quinazolin-4-one (5), which can be treated with thionyl chloride to yield 4-chloro-6-nitro-7-fluoro-3H-quinazoline (6). The 4-chloro-quinazoline compound (6) can be combined with a desirably substituted aniline, represented above by 4-fluoro-3-chloro-aniline, in the presence of a tertiary amine and isopropanol to provide the 4-anilino-6-nitro-7-fluoro-quinazoline (7).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08623883B2 |
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| 출처 데이터셋 | uspto-grants-2014_01 |
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| ORD ID | ord-5939c849420149fa8a0b323f9319daef |
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| 출처 메모 | uspto-grants-2014_01 |
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