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

HRID 1060789ノート

反応式

HRID 1060789 の反応式
[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

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

  1. customwas placed in a preheated oil bath at 90° C
  2. customAfter 10 minutes a clear yellow melt was formed and after a further 20 minutes the mixture
  3. customDecantation and evaporation in vacuo
  4. customgave a residue which
  5. 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

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