Methyl 1-ethylindole-3-carboxylate → 3-(1-Ethyl-1H-indol-3-yl)-3-oxo-propionitrile
반응식
[NH2:1][C:2]1[CH:6]=CNN=1.CO[C:9]([C:11]1[C:19]2[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=2)[N:13]([CH2:20][CH3:21])[CH:12]=1)=[O:10]>>[CH2:20]([N:13]1[C:14]2[C:19](=[CH:18][CH:17]=[CH:16][CH:15]=2)[C:11]([C:9](=[O:10])[CH2:6][C:2]#[N:1])=[CH:12]1)[CH3:21]참가 물질
3
실험 절차
The product was prepared according to the general procedure for aminopyrazole synthesis (route A1bis) from 1-ethyl-1H-indole-3-carboxylic acid methyl ester (860.0 mg, 4.2 mmol, 1.0 eq). 820.0 mg of the title product (yield 91%) were obtained and used directly for the next step.
후처리
- customThe product was prepared
출처 및 근거
- ORD 기록
- ord-fb38623cd966453292ae4a72f843fb58
- 출처 데이터셋
- uspto-grants-2012_04
- 특허 번호
- US08163729B2
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