反応式
[CH2:1]([NH:5][C:6](=[O:44])[O:7][CH2:8][CH:9]1[CH2:14][CH2:13][CH:12]([CH2:15][N:16]([CH2:37][C:38]2[CH:43]=[CH:42][CH:41]=[CH:40][CH:39]=2)[S:17]([NH:20][C:21](=[O:36])[C:22]2[CH:27]=[C:26]([C:28]([F:31])([F:30])[F:29])[CH:25]=[C:24]([C:32]([F:35])([F:34])[F:33])[CH:23]=2)(=[O:19])=[O:18])[CH2:11][CH2:10]1)[CH2:2][CH2:3][CH3:4].[CH3:45]C(N)CCC.C(N)CCC>>[CH3:45][CH:1]([NH:5][C:6](=[O:44])[O:7][CH2:8][CH:9]1[CH2:10][CH2:11][CH:12]([CH2:15][N:16]([CH2:37][C:38]2[CH:43]=[CH:42][CH:41]=[CH:40][CH:39]=2)[S:17]([NH:20][C:21](=[O:36])[C:22]2[CH:23]=[C:24]([C:32]([F:35])([F:33])[F:34])[CH:25]=[C:26]([C:28]([F:30])([F:29])[F:31])[CH:27]=2)(=[O:18])=[O:19])[CH2:13][CH2:14]1)[CH2:2][CH2:3][CH3:4]参加物
4
実験手順
Following the procedure to make (13), 1-methylbutyl amine was substituted for butyl amine to give the title compound after purification. 1H NMR (500 MHz, DMSO-d6): δ 8.45 (s, 2H), 8.12 (s, 1H), 7.37 (d, 2H), 7.24 (t, 2H), 7.17 (t, 1H), 6.79 (d, 1H), 4.35 (s, 2H), 3.60 (d, 2H), 3.41 (m, 1H), 3.30 (water), 2.89 (d, 2H), 2.48 (DMSO), 1.62 (m, 2H), 1.55 (m, 2H), 1.34-1.19 (m, 6H), 0.96 (d, 3H), 0.80 (t, 3H), 0.62 (m, 4H).
出典と根拠
- ORDレコード
- ord-3258c750fc7a4b7b9b41b2bdbdd04b43
- 出典データセット
- uspto-grants-2005_02
- 特許番号
- US06852738B2
関連ノート
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