2-(3,4-Dichlorophenyl)-2-hydroxyacetic acid → N-[(7-methoxy-1,2,3,4-tetrahydronaphth-2-yl) methyl]-3,4-dichloromandelamide
反応式
[Cl:1][C:2]1[CH:3]=[C:4]([CH:10]=[CH:11][C:12]=1[Cl:13])[CH:5]([OH:9])[C:6]([OH:8])=O.[NH2:14][CH2:15][CH:16]1[CH2:25][CH2:24][C:23]2[C:18](=[CH:19][C:20]([O:26][CH3:27])=[CH:21][CH:22]=2)[CH2:17]1>>[CH3:27][O:26][C:20]1[CH:19]=[C:18]2[C:23]([CH2:24][CH2:25][CH:16]([CH2:15][NH:14][C:6](=[O:8])[CH:5]([C:4]3[CH:10]=[CH:11][C:12]([Cl:13])=[C:2]([Cl:1])[CH:3]=3)[OH:9])[CH2:17]2)=[CH:22][CH:21]=1参加物
3
実験手順
By following the procedure of Example 1(i) but starting from 3,4-dichloromandelic acid (3.1 g, 0.014 mol) and 2-aminomethyl-7-methoxy-1,2,3,4-tetrahydronaphthalene (2.67 g, 0.014 mol), N-[(7-methoxy-1,2,3,4-tetrahydronaphth-2-yl) methyl]-3,4-dichloromandelamide (4.5 g) is obtained as an oily product characterised by the following IR absorption maxima 3380 (b): O--H, CON--H; and 1641: NHC=0 cm-1.
出典と根拠
- ORDレコード
- ord-22ee088bbeaa479aadbdeaed4f272c76