反応式
[CH2:1]([N:3]([CH2:6][C:7]1[O:15][C:14]2[CH2:13][CH2:12][N:11]([C:16](=[O:28])[CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][C:22]3[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=3)[CH2:10][C:9]=2[CH:8]=1)[CH2:4][CH3:5])[CH3:2].[ClH:29]>CO>[ClH:29].[CH2:1]([N:3]([CH2:6][C:7]1[O:15][C:14]2[CH2:13][CH2:12][N:11]([C:16](=[O:28])[CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][C:22]3[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=3)[CH2:10][C:9]=2[CH:8]=1)[CH2:4][CH3:5])[CH3:2]参加物
4
実験手順
1-(2-Diethylaminomethyl-6,7-dihydro-4H-furo[3,2-c]pyridin-5-yl)-6-phenylhexan-1-one 0.209 g was dissolved in 2 ml of methanol; hydrogen chloride in methanol was added in excess, followed by stirring. After this mixture was concentrated, diethyl ether was added; the resulting solid was filtered and washed with diethyl ether to yield the desired product.
後処理
- concentrationAfter this mixture was concentrated
- additiondiethyl ether was added
- filtrationthe resulting solid was filtered
- washwashed with diethyl ether
出典と根拠
- ORDレコード
- ord-25c02bd397284bc1bb5b1ce461bbeba8
- 出典データセット
- uspto-grants-1999_12
- 特許番号
- US05998433
関連ノート
読み込み中…