反応式
[CH3:1][N:2]([CH2:4][C:5]1[O:13][C:12]2[CH2:11][CH2:10][N:9]([C:14](=[O:29])/[C:15](/[C:23]3[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=3)=[CH:16]/[C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)[CH2:8][C:7]=2[CH:6]=1)[CH3:3].[ClH:30]>CO.C(OCC)(=O)C>[ClH:30].[CH3:1][N:2]([CH2:4][C:5]1[O:13][C:12]2[CH2:11][CH2:10][N:9]([C:14](=[O:29])/[C:15](/[C:23]3[CH:24]=[CH:25][CH:26]=[CH:27][CH:28]=3)=[CH:16]/[C:17]3[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=3)[CH2:8][C:7]=2[CH:6]=1)[CH3:3]参加物
5
反応物 2
生成物 1
試薬・触媒・溶媒 2
実験手順
(E)-N,N-Dimethyl-[5-(2,3-diphenylpropenoyl)-4,5,6,7-tetrahydrofuro[3,2-c]pyridin-2-ylmethyl]amine 0.241 g was dissolved in 2 ml of methanol; hydrogen chloride in ethyl acetate was added in excess, followed by stirring. This mixture was concentrated and washed with diethyl ether to yield the desired product.
後処理
- concentrationThis mixture was concentrated
- washwashed with diethyl ether
出典と根拠
- ORDレコード
- ord-1c20908060a24e9a8f283d8a87b7543b
- 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…