2-(5-methoxy-1H-indol-3-yl)-1-(toluene-4-sulfonyl)-1H-pyrrolo[2,3-b]pyridine-4-carbonitrile → 2-(5-Methoxy-1H-indol-3-yl)-1H-pyrrolo[2,3-b]pyridine-4-carbonitrile
反応式
IC1N(S(C2C=CC(C)=CC=2)(=O)=O)C2N=CC=C(C#N)C=2C=1.[CH3:23][O:24][C:25]1[CH:26]=[C:27]2[C:31](=[CH:32][CH:33]=1)[NH:30][CH:29]=[C:28]2[C:34]1[N:44](S(C2C=CC(C)=CC=2)(=O)=O)[C:37]2[N:38]=[CH:39][CH:40]=[C:41]([C:42]#[N:43])[C:36]=2[CH:35]=1>C(OCC)(=O)C.CCCCCCC>[CH3:23][O:24][C:25]1[CH:26]=[C:27]2[C:31](=[CH:32][CH:33]=1)[NH:30][CH:29]=[C:28]2[C:34]1[NH:44][C:37]2[N:38]=[CH:39][CH:40]=[C:41]([C:42]#[N:43])[C:36]=2[CH:35]=1参加物
4
反応物 2
生成物 1
試薬・触媒・溶媒 1
実験手順
By proceeding in a similar manner to Reference Example 12(a) but using 2-iodo-1-(toluene-4-sulfonyl)-1H-pyrrolo[2,3-b]pyridine-4-carbonitrile [Reference Example 62(a)] there was prepared the title compound as a yellow solid, m.p. 303–304° C., TLC RF=0.07 (ethyl acetate/heptane 1:1) and 2-(5-methoxy-1H-indol-3-y)-1-(toluene-4-sulfonyl)-1H-pyrrolo[2,3-b]pyridine-4-carbonitrile [Reference Example 100] as a brown oil. MS: 443 (MH+). TLC: RF=0.38 (ethyl acetate/heptane 1:1).
出典と根拠
- ORDレコード
- ord-ba5cdb8dfcaf41f68bc62f7bb27f2626
- 出典データセット
- uspto-grants-2007_06
- 特許番号
- US07227020B2
反応ノート
読み込み中…