Diethyl Ether → N-[1-(alpha-(2-(2-(2-Methoxyethoxy)-ethoxy)-ethoxycarbonyloxy)benzyl)-1,4-dihydropyridin-4-ylidene]-N'-cyano-N''-(6-(4-chlorophenoxy)-hexyl)-guanidine
反応式
[Cl:1][C:2]1[CH:26]=[CH:25][C:5]([O:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][NH:13][C:14]([NH:22][C:23]#[N:24])=[N:15][C:16]2[CH:21]=[CH:20][N:19]=[CH:18][CH:17]=2)=[CH:4][CH:3]=1.[C:27](=[O:48])([O:37][CH2:38][CH2:39][O:40][CH2:41][CH2:42][O:43][CH2:44][CH2:45][O:46][CH3:47])[O:28][CH:29](Cl)[C:30]1[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=1.CCOC(C)=O.CCOCC>ClCCl>[CH3:47][O:46][CH2:45][CH2:44][O:43][CH2:42][CH2:41][O:40][CH2:39][CH2:38][O:37][C:27]([O:28][CH:29]([N:19]1[CH:20]=[CH:21][C:16](=[N:15][C:14]([NH:22][C:23]#[N:24])=[N:13][CH2:12][CH2:11][CH2:10][CH2:9][CH2:8][CH2:7][O:6][C:5]2[CH:25]=[CH:26][C:2]([Cl:1])=[CH:3][CH:4]=2)[CH:17]=[CH:18]1)[C:30]1[CH:31]=[CH:32][CH:33]=[CH:34][CH:35]=1)=[O:48]参加物
6
反応物 4
生成物 1
試薬・触媒・溶媒 1
実験手順
A mixture of N-(6-(4-chlorophenoxy)-hexyl)-N′-cyano-N″-(4-pyridyl)-guanidine (67 mg) and α-chlorobenzyl 2-(2-(2-methoxyethoxy)-ethoxy)-ethyl carbonate (150 mg) was placed in a preheated oil bath at 90° C. After 10 minutes a clear yellow melt was formed and after a further 20 minutes the mixture was cooled to room temperature and EtOAc (4 ml) was added. Decantation and evaporation in vacuo gave a residue which was treated with ether. After decantation of the ether, the residue was taken up in dichloromethane and washed with an excess of sodium bicarbonate. Chromatography on silica gel with dichloromethane/methanol (98:2) as eluent gave the title compound as a colourless oil.
後処理
- customwas placed in a preheated oil bath at 90° C
- customAfter 10 minutes a clear yellow melt was formed and after a further 20 minutes the mixture
- customDecantation and evaporation in vacuo
- customgave a residue which
- washwashed with an excess of sodium bicarbonate
出典と根拠
- ORDレコード
- ord-5e422d87fc5f4d0882780eb4bd096495
- 出典データセット
- uspto-grants-2003_02
- 特許番号
- US06525077B2
反応ノート
読み込み中…