反応式
[CH3:1][C:2]1[C:3]2[C:8]([CH:9]3[C:14]=1[CH2:13][CH2:12][NH:11][CH2:10]3)=[CH:7][CH:6]=[CH:5][CH:4]=2.[C:15]1([NH:21][C:22](=[O:25])[CH:23]=[CH2:24])[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1.Cl>>[CH3:1][C:2]1[C:3]2[C:8]([CH:9]3[C:14]=1[CH2:13][CH2:12][N:11]([CH2:24][CH2:23][C:22]([NH:21][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)=[O:25])[CH2:10]3)=[CH:7][CH:6]=[CH:5][CH:4]=2参加物
4
実験手順
1,3,4,9b-Tetrahydro-5-methyl-2H-indeno[1,2-c]pyridine and N-phenyl acrylamide are reacted in accordance with the process described in Example 6. Reaction period 4 hours. M.P. of the hydrochloride of the title compound 207°-209° from 95% ethanol.
後処理
- customReaction period 4 hours
出典と根拠
- ORDレコード
- ord-dfd3edd2b6e24ecda950bbbca3bb4bba
- 出典データセット
- uspto-grants-1976_11
- 特許番号
- US03991066
関連ノート
読み込み中…