참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetonitrile | HCID 6342 | — |
| 반응물 | 3-(Dimethylamino)benzoic acid | HCID 66837 | — |
| 반응물 | 7-Chloro-1,8-naphthyridin-2-amine | HCID 85199 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | N-(7-Chloro-1,8-naphthyridin-2-yl)-3-dimethylaminobenzamide | HCID 20217506 | 63.1% |
반응 단계
The procedure is similar to that described in Example 1, but starting with 3-dimethylaminobenzoic acid (6.6 g), N,N'-carbonyldiimidazole (6.5 g) and 2-amino-7-chloro-1,8-naphthyridine (5.4 g). The product produced by precipitation in water (9 g; m.p. 212° C.) is dissolved in boiling acetonitrile (400 cc). After 3 hours' cooling at 4° C., the crystallised solid is separated by filtration, washed with acetonitrile (3×20 cc) and dried at 40° C. under reduced pressure (0.067 kPa). N-(7-Chloro-1,8-naphthyridin-2-yl)-3-dimethylaminobenzamide (6.2 g) is produced, m.p. 215° 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-7e60164d16154487bf86938c319458e4 |
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| 출처 메모 | uspto-grants-1987_02 |
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