4-Methoxybenzyl alcohol → tert-butyl N-[(4-methoxyphenyl)methyl]-N-[(E)-N-[(2-methylpropan-2-yl)oxycarbonyl]-C-pyrazol-1-ylcarbonimidoyl]carbamate
反応式
[C:1]([O:5][C:6](=[O:33])[N:7](/[C:19](=[N:25]/[C:26]([O:28][C:29]([CH3:32])([CH3:31])[CH3:30])=[O:27])/[N:20]1[CH:24]=[CH:23][CH:22]=[N:21]1)[CH2:8]CCC1C=CC(OC)=CC=1)([CH3:4])([CH3:3])[CH3:2].[CH3:34][O:35][C:36]1[CH:43]=[CH:42][C:39](CO)=[CH:38][CH:37]=1>>[C:1]([O:5][C:6](=[O:33])[N:7](/[C:19](=[N:25]\[C:26]([O:28][C:29]([CH3:30])([CH3:31])[CH3:32])=[O:27])/[N:20]1[CH:24]=[CH:23][CH:22]=[N:21]1)[CH2:8][C:39]1[CH:42]=[CH:43][C:36]([O:35][CH3:34])=[CH:37][CH:38]=1)([CH3:4])([CH3:2])[CH3:3]参加物
3
反応物 2
生成物 1
実験手順
The title compound is prepared by an analogous procedure to Intermediate E by replacing 3-(4-methoxyphenyl)-1-propanol with 4-methoxybenzylalcohol. [M+H]+ 431.
出典と根拠
- ORDレコード
- ord-eaabfc901ab64574a275935f75e21024
- 出典データセット