참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 3-Chloroaniline | HCID 7932 | — |
| 반응물 | Hexane | HCID 8058 | — |
| 반응물 | 4-Chloro-7-fluoro-6-nitroquinazoline | HCID 10609358 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 용매 | 1,4-Dioxane | HCID 31275 | — |
| 생성물 | 4-[(3-Chlorophenyl)amino]-7-fluoro-6-nitro-quinazoline | HCID 22270087 | — |
반응 단계
A solution of 2.76 ml of 3-chloroaniline in 7 ml of dioxan is added dropwise to 5.0 g of 4-chloro-7-fluoro-6-nitro-quinazoline in 40 ml of methylene chloride at 15° C. within 15 minutes. The reaction mixture is stirred for a further 15 minutes at this temperature before being poured onto 100 ml of n-hexane for working up. The mixture is stirred for about one hour while cooling with an ice bath, then the precipitate formed is filtered off. The hydrochloride thus obtained is suspended in 30 ml of methanol, made alkaline with triethylamine while cooling with an ice bath and combined with 100 ml of water. The precipitate formed is suction filtered and washed with water. The crude product is purified by chromatography on a silica gel column with methylene chloride/methanol (20:1) as eluant. Yield: 3.50 g (50% of theory), Melting point: 223-225° C. Mass spectrum (ESI*): m/z=319, 321 [M+H]*
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06972288B1 |
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| 출처 데이터셋 | uspto-grants-2005_12 |
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| ORD ID | ord-9ad4d352327a47ab8d31988f0e557e3c |
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| 출처 메모 | uspto-grants-2005_12 |
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