Hydrochloric Acid → 2,3-Dimethyl-5-methylthio-7-phenacylpyrrolo[2,3-b]pyridine
反応式
[CH3:1][C:2]1[NH:12][C:5]2=[N:6][CH:7]=[C:8]([S:10][CH3:11])[CH:9]=[C:4]2[C:3]=1[CH3:13].CC1NC2=NC(SC)=CC=C2C=1C.[CH2:27](Cl)[C:28]([C:30]1[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=1)=[O:29].Cl>>[CH3:1][C:2]1[N:12]=[C:5]2[N:6]([CH2:27][C:28]([C:30]3[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=3)=[O:29])[CH:7]=[C:8]([S:10][CH3:11])[CH:9]=[C:4]2[C:3]=1[CH3:13]参加物
5
実験手順
The title compound was prepared on a 0.6 mmol scale from 2,3-dimethyl-5-methylthiopyrrolo[2,3-b]pyridine (prepared according to the procedure described for 2,3-dimethyl-6-methylthio-pyrrolo[2,3-b]pyridine) and phenacyl chloride as described in Example 43 yielding 140 mg (63%) pure title compound as the hydrochloride.
後処理
- customprepared
出典と根拠
- ORDレコード
- ord-3d14531c529746d9b83f1643dae5288f
- 出典データセット
- uspto-grants-1995_08
- 特許番号
- US05439917
反応ノート
読み込み中…