tert-Butyl 3-amino-1H-pyrazole-1-carboxylate → 3-(3-Benzyloxy-5-isopropoxy-benzoylamino)-pyrazole-1-carboxylic acid tert-butyl ester
反応式
[CH3:1][CH:2]([O:4][C:5]1[CH:6]=[C:7]([CH:11]=[C:12]([O:14][CH2:15][C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)[CH:13]=1)[C:8]([OH:10])=O)[CH3:3].[NH2:22][C:23]1[CH:27]=[CH:26][N:25]([C:28]([O:30][C:31]([CH3:34])([CH3:33])[CH3:32])=[O:29])[N:24]=1>>[CH3:3][CH:2]([O:4][C:5]1[CH:6]=[C:7]([C:8]([NH:22][C:23]2[CH:27]=[CH:26][N:25]([C:28]([O:30][C:31]([CH3:34])([CH3:33])[CH3:32])=[O:29])[N:24]=2)=[O:10])[CH:11]=[C:12]([O:14][CH2:15][C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)[CH:13]=1)[CH3:1]参加物
3
実験手順
The preparations of 3-[(1-methylethyl)oxy]-5-[(phenylmethyl)oxy]benzoic acid and 1,1-dimethylethyl 3-amino-1H-pyrazole-1-carboxylate were described earlier.
出典と根拠
- ORDレコード
- ord-2213c70bd844469cb02c7e2cb03e4b98
- 出典データセット
- uspto-grants-2010_11
- 特許番号
- US07842694B2