3-(Oxiran-2-yl)pyridine → HCID 20073151、化合物

反応式

[O:1]1[CH2:3][CH:2]1[C:4]1[CH:5]=[N:6][CH:7]=[CH:8][CH:9]=1.[NH2:10][CH:11]([CH3:22])[CH2:12][CH2:13][C:14]1[S:18][C:17]([C:19]([NH2:21])=[O:20])=[CH:16][CH:15]=1>CS(C)=O.O>[OH:1][CH:2]([C:4]1[CH:5]=[N:6][CH:7]=[CH:8][CH:9]=1)[CH2:3][NH:10][CH:11]([CH3:22])[CH2:12][CH2:13][C:14]1[S:18][C:17]([C:19]([NH2:21])=[O:20])=[CH:16][CH:15]=1

参加物

実験手順

606 mg of 3-[(RS)-2-oxiranyl]pyridine and 991 mg of (RS)-5-(3-aminobutyl)-2-thiophenecarboxamide were heated to 100° for 25 hours in 5 ml of DMSO. The reaction mixture was diluted with water and extracted three times with methylene chloride. The methylene chloride solutions were washed with water, dried and evaporated in a vacuum. Chromatography of the residue on silica gel with ether/methanol gave 149 mg of 5-[(RS)-3-[[(RS)-2-hydroxy-2-(3-pyridyl)ethyl]amino]butyl]-2-thiophenecarboxamide, ε201 =14420; ε268 =11310.