3,5-diethyl 4-iodo-1H-pyrazole-3,5-dicarboxylate → 1-(2-tert-Butoxycarbonylamino-ethyl)-4-iodo-1H-pyrazole-3,5-dicarboxylic acid diethyl ester
反応式
[CH2:1]([O:3][C:4]([C:6]1[C:10]([I:11])=[C:9]([C:12]([O:14][CH2:15][CH3:16])=[O:13])[NH:8][N:7]=1)=[O:5])[CH3:2].C(OC(C1N([CH2:35][CH2:36][NH:37][C:38]([O:40][C:41]([CH3:44])([CH3:43])[CH3:42])=[O:39])N=C(COC2C=CC=CC=2)C=1)=O)C>>[CH2:1]([O:3][C:4]([C:6]1[C:10]([I:11])=[C:9]([C:12]([O:14][CH2:15][CH3:16])=[O:13])[N:8]([CH2:35][CH2:36][NH:37][C:38]([O:40][C:41]([CH3:44])([CH3:43])[CH3:42])=[O:39])[N:7]=1)=[O:5])[CH3:2]参加物
3
実験手順
The compound was prepared from 4-iodo-1H-pyrazole-3,5-dicarboxylic acid diethyl ester and 2-(2-tert-butoxycarbonylamino)ethyl bromide using the method described in the preceding example 5 (2-(2-tert-butoxycarbonylamino-ethyl)-5-phenoxymethyl-2H-pyrazole-3-carboxylic acid ethyl ester).
出典と根拠
- ORDレコード
- ord-f42d332cd7b6453a8beec81efeb796c8