HCID 861823、化合物 → 5-Phenyl-7,8-dihydro-[1,3]dioxolo[4,5-g]isoquinoline
反応式
[CH2:1]1[O:20][C:19]2[CH:18]=[CH:17][C:5]([CH2:6][CH2:7][NH:8][C:9](=O)[C:10]3[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=3)=[CH:4][C:3]=2[O:2]1.[CH2:21]1[CH2:41][O:40][C:39]2[CH:38]=[CH:37][C:25]([CH2:26][CH2:27][NH:28][C:29](=O)[C:30]3[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=3)=[CH:24][C:23]=2[O:22]1>>[CH2:1]1[O:20][C:19]2[CH:18]=[C:17]3[C:5]([CH2:6][CH2:7][N:8]=[C:9]3[C:10]3[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=3)=[CH:4][C:3]=2[O:2]1.[CH2:21]1[CH2:41][O:40][C:39]2[CH:38]=[C:37]3[C:25]([CH2:26][CH2:27][N:28]=[C:29]3[C:30]3[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=3)=[CH:24][C:23]=2[O:22]1参加物
4
実験手順
Substitution of an equivalent quantity of N-(3,4-methylenedioxyphenethyl)benzamide or N-(3,4-ethylenedioxyphenethyl)benzamide for the substituted benzamide called for in the first paragraph of this example and substantial repetition of the procedure there detailed affords 6,7-methylenedioxy-1-phenyl-3,4-dihydroisoquinoline or 6,7-ethylenedioxy-1-phenyl-3,4-dihydroisoquinoline, respectively.
出典と根拠
- ORDレコード
- ord-5d1714b456e84f3d8d45d2fc11e591c8