참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | trans-3-[2-(7-Chloroquinolin-2-yl)ethenyl]benzyl chloride | HCID 19369489 | — |
| 반응물 | 3-(1H-Indol-7-YL)propanenitrile | HCID 19959105 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | HCID 19102601 | HCID 19102601 | — |
반응 단계
A solution of 7-(2-cyanoethyl)indole (Example 14a) (4.42 g, 26 mmol) in dimethylformamide (30 ml) was added dropwise to a stirred suspension of sodium hydride (1.3 g, 60% dispersion, 32.5 mmol, washed with hexane under nitrogen) in dimethylformamide (30 ml) at 10°-15° C. The mixture was stirred for 15 minutes at ca 15° C. then a suspension of 3-[2(E)-(7-chloroquinolin-2-yl)ethenyl] benzyl chloride (Example 14b) (10.2 g, 32.5 mmol) in dimethylformamide (60 ml) was added rapidly. The dark mixture was stirred for 5 hours at room temperature, poured onto saturated ammonium chloride solution and extracted with dichloromethane. The extract was dried and evaporated under high vacuum and the residue in dichloromethane (30 ml) was applied to a silica column and eluted with ethyl acetate-hexane (1:2). The product was recrystallised from ethyl acetate-hexane, m.p. 151° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05281593 |
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| 출처 데이터셋 | uspto-grants-1994_01 |
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| ORD ID | ord-f6249be6704b456aaa971ddb5179a7e7 |
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| 출처 메모 | uspto-grants-1994_01 |
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