반응식
[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([C:7]2[NH:8][C:9]3[C:14]([CH:15]=2)=[CH:13][C:12]([C:16]#[N:17])=[CH:11][CH:10]=3)[CH:2]=1.C(O[C:23]([C:25]1[CH:33]=[CH:32][C:28]([C:29]([OH:31])=O)=[CH:27][CH:26]=1)=[O:24])CCC.C1CCC(N=C=N[CH:43]2[CH2:48][CH2:47]CCC2)CC1.[OH2:49].[CH3:50]N(C=O)C>CN(C1C=CN=CC=1)C>[C:48]([O:49][C:23](=[O:24])[C:25]1[CH:26]=[CH:27][C:28]([C:29]([N:8]2[C:9]3[C:14](=[CH:13][C:12]([C:16]#[N:17])=[CH:11][CH:10]=3)[CH:15]=[C:7]2[C:3]2[CH:2]=[N:1][CH:6]=[CH:5][CH:4]=2)=[O:31])=[CH:32][CH:33]=1)([CH3:47])([CH3:43])[CH3:50]참가 물질
7
반응물 5
생성물 1
시약·촉매·용매 1
실험 절차
To 2-pyridin-3-yl-1H-indole-5-carbonitrile (575 mg, 2.62 mmol), 4-(butoxycarbonyl)benzoic acid (700 mg, 3.15 mmol) and DMAP (780 mg, 3.93 mmol) in DMF (30 mL) is added DCC (811 mg, 3.93 mmol). The reaction is stirred for 3 days and the mixture is poured into water (50 mL) and extracted with ethyl acetate, dried over Na2SO4 and concentrated. The residue is purified by silica gel flash chromatography (ethyl acetate-heptane gradient) to give 4-(5-cyano-2-pyridin-3-yl-indole-1-carbonyl)-benzoic acid tert-butyl ester as a white solid. MS (ESI) m/z 424 (M+H)+.
후처리
- extractionextracted with ethyl acetate
- dry with materialdried over Na2SO4
- concentrationconcentrated
- customThe residue is purified by silica gel flash chromatography (ethyl acetate-heptane gradient)
출처 및 근거
- ORD 기록
- ord-246ac85c300343d3bd1c155dba15a7b9
- 출처 데이터셋
- uspto-grants-2011_10
- 특허 번호
- US08030334B2
연결된 노트
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