참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethanol | HCID 702 | — |
| 반응물 | 7-Chloro-1,8-naphthyridin-2-amine | HCID 85199 | — |
| 반응물 | 1,4-Cyclohexadiene-1-carboxylic acid | HCID 297211 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | N-(7Chloro-1,8-naphthyridin-2-yl)-1,4-cyclohexadiene-1-carboxamide | HCID 20217543 | 33% |
반응 단계
The procedure is similar to that described in Example 1, but starting with 1,4-cyclohexadiene-1-carboxylic acid (6.2 g), N,N'-carbonyldiimidazole (8 g) and 2-amino-7-chloro-1,8-naphthyridine (8 g). The product produced by precipitation in water (11 g; m.p. 205° C.) is dissolved in boiling ethanol (250 cc). After 2 hours' cooling at 4° C., the crystallised solid is separated by filtration, washed with ethanol (3×15 cc) and dried at 40° C. under reduced pressure (0.067 kPa). N-(7Chloro-1,8-naphthyridin-2-yl)-1,4-cyclohexadiene-1-carboxamide (4.2 g) is produced, m.p. 210° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04642308 |
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| 출처 데이터셋 | uspto-grants-1987_02 |
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| ORD ID | ord-67f63937ad5640b7979af9cf1aff7358 |
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| 출처 메모 | uspto-grants-1987_02 |
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