反応式
C([O:8][C:9]1[CH:10]=[C:11]([CH:23]=[C:24]([O:26][C@@H:27]([CH3:37])[CH2:28][O:29][Si:30]([C:33]([CH3:36])([CH3:35])[CH3:34])([CH3:32])[CH3:31])[CH:25]=1)[C:12]([NH:14][C:15]1[CH:19]=[CH:18][N:17]([CH:20]([CH3:22])[CH3:21])[N:16]=1)=[O:13])C1C=CC=CC=1>C1COCC1>[Si:30]([O:29][CH2:28][C@H:27]([CH3:37])[O:26][C:24]1[CH:23]=[C:11]([CH:10]=[C:9]([OH:8])[CH:25]=1)[C:12]([NH:14][C:15]1[CH:19]=[CH:18][N:17]([CH:20]([CH3:21])[CH3:22])[N:16]=1)=[O:13])([C:33]([CH3:35])([CH3:36])[CH3:34])([CH3:32])[CH3:31]参加物
3
反応物 1
生成物 1
試薬・触媒・溶媒 1
実験手順
A solution of 3-(benzyloxy)-5-((1S)-2-{[tert-butyl(dimethyl)silyl]oxy}-1-methylethoxy)-N-(1-isopropyl-1H-pyrazol-3-yl)benzamide (1.97 g, 3.77 mmol) and THF (70 mL) was evacuated and purged with, Argon (×3). Palladium on carbon (10% w/w, 400 mg) was added and reaction mixture was evacuated and finally purged with hydrogen gas. Reaction mixture was left to stir at ambient temperature under hydrogen for 16 hours. Pd/C was filtered off and concentrated in vacuo to give the product as a colourless oil (1.58 g, 97%).
後処理
- custompurged with, Argon (×3)
- additionPalladium on carbon (10% w/w, 400 mg) was added
- customreaction mixture
- customwas evacuated
- customfinally purged with hydrogen gas
- customReaction mixture
- waitwas left
- filtrationPd/C was filtered off
- concentrationconcentrated in vacuo
出典と根拠
- ORDレコード
- ord-09e532e382744faebd128349e8aaedc0
- 出典データセット
- uspto-grants-2010_06
- 特許番号
- US07745475B2
関連ノート
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