HCID 18782313、化合物 → HCID 22458120、化合物
反応式
[CH:1]1([C:7]([N:9]([C:27]2[CH:32]=[CH:31][CH:30]=[CH:29][C:28]=2[O:33][C:34]([F:37])([F:36])[F:35])[CH2:10][CH2:11][N:12]2[CH2:17][CH2:16][N:15]([C:18]3[CH:23]=[CH:22][C:21]([NH2:24])=[CH:20][C:19]=3[O:25][CH3:26])[CH2:14][CH2:13]2)=[O:8])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.NC1C=CC=CC=1N(C(C1CCCCC1)=O)CCN1CCN([C:54]2C=CC=C[C:55]=2[O:60]C)CC1>>[CH:1]1([C:7]([N:9]([C:27]2[CH:32]=[CH:31][CH:30]=[CH:29][C:28]=2[O:33][C:34]([F:36])([F:37])[F:35])[CH2:10][CH2:11][N:12]2[CH2:13][CH2:14][N:15]([C:18]3[CH:23]=[CH:22][C:21]([NH:24][C:55](=[O:60])[CH3:54])=[CH:20][C:19]=3[O:25][CH3:26])[CH2:16][CH2:17]2)=[O:8])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1参加物
3
実験手順
The title compound was synthesized according to the procedure reported in example 28 but substituting the compound of example 56 for the compound of example 27 and stirring for 20 h. The residue was purified by flash chromatography (CHCl3-2 N methanolic NH3 100:3) affording the title compound as a vitreous pink solid. Yield: 77%.
後処理
- customThe title compound was synthesized
- customThe residue was purified by flash chromatography (CHCl3-2 N methanolic NH3 100:3)
出典と根拠
- ORDレコード
- ord-9223298adfc342b08f04aaaec7b792ac