HCID 10703813、化合物 → HCID 131719231、化合物
反応式
[F:1][C:2]1[CH:20]=[CH:19][C:5]2[C:6]([CH:9]3[CH2:14][CH2:13][N:12]([CH2:15][CH2:16][CH2:17][OH:18])[CH2:11][CH2:10]3)=[N:7][O:8][C:4]=2[CH:3]=1.[CH3:21][N:22]([C:26]1[CH:31]=[CH:30][C:29]2[O:32][CH2:33][O:34][C:28]=2[CH:27]=1)[C:23]([Cl:25])=[O:24]>>[ClH:25].[F:1][C:2]1[CH:20]=[CH:19][C:5]2[C:6]([CH:9]3[CH2:14][CH2:13][N:12]([CH2:15][CH2:16][CH2:17][O:18][C:23](=[O:24])[N:22]([CH3:21])[C:26]4[CH:31]=[CH:30][C:29]5[O:32][CH2:33][O:34][C:28]=5[CH:27]=4)[CH2:11][CH2:10]3)=[N:7][O:8][C:4]=2[CH:3]=1参加物
3
実験手順
By following the procedure described in example 2B 3-(4-(6-fluoro -1,2-benzisoxazol-3-yl)piperidino)propanol (278 mg, 1 mmol) was reacted with N-methyl-N-(3,4-methylenedioxyphenyl)carbamoylchloride (240 mg, 1.12 mmol) to give 170 mg of the title compound. M.p. 126°-129° C.
出典と根拠
- ORDレコード
- ord-57437141a9de4cd6b0befe9b0b0de902
- 出典データセット
- uspto-grants-1995_12
- 特許番号