Hydrochloric Acid → 1-(4-fluoro-1-indan-1-ylpiperidin-4-yl)-1,3-dihydro-2H-benzimidazol-2-one hydrochloride
反応式
FC1C=CC=C2C=1CCC2=O.[F:12][C:13]1([N:28]2[C:32]3[CH:33]=[CH:34][CH:35]=[CH:36][C:31]=3[NH:30][C:29]2=[O:37])[CH2:18][CH2:17][N:16]([CH:19]2[C:27]3[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=3)[CH2:21][CH2:20]2)[CH2:15][CH2:14]1.[ClH:38].Cl.C(OCC)(=O)C>>[ClH:38].[F:12][C:13]1([N:28]2[C:32]3[CH:33]=[CH:34][CH:35]=[CH:36][C:31]=3[NH:30][C:29]2=[O:37])[CH2:18][CH2:17][N:16]([CH:19]2[C:27]3[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=3)[CH2:21][CH2:20]2)[CH2:15][CH2:14]1参加物
5
実験手順
In the same manner as in Example 1 and using 4-fluoro-1-indanone, 1-(4-fluoro-1-indan-1-ylpiperidin-4-yl)-1,3-dihydro-2H-benzimidazol-2-one was synthesized, which was then converted to hydrochloride with 4N hydrochloric acid-ethyl acetate solution to give the title compound as a brown solid.
後処理
- customwas synthesized
出典と根拠
- ORDレコード
- ord-0077fe4cb168461a9abbb4d6f050a39b
- 出典データセット
- uspto-grants-2014_11
- 特許番号
- US08877779B2
反応ノート
読み込み中…