Potassium Sodium Tartrate → (6-(Benzyloxy)-1-(tetrahydro-2H-pyran-2-yl)indazol-3-yl)methanol
反応式
C([O:3][C:4]([C:6]1[C:14]2[C:9](=[CH:10][C:11]([O:15][CH2:16][C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)=[CH:12][CH:13]=2)[N:8]([CH:23]2[CH2:28][CH2:27][CH2:26][CH2:25][O:24]2)[N:7]=1)=O)C.[H-].[H-].[H-].[H-].[Li+].[Al+3].[C@H](O)(C([O-])=O)[C@@H](O)C([O-])=O.[Na+].[K+].C(=O)([O-])O.[Na+]>C1COCC1.C1COCC1.O>[CH2:16]([O:15][C:11]1[CH:10]=[C:9]2[C:14]([C:6]([CH2:4][OH:3])=[N:7][N:8]2[CH:23]2[CH2:28][CH2:27][CH2:26][CH2:25][O:24]2)=[CH:13][CH:12]=1)[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1参加物
反応物 4
生成物 1
試薬・触媒・溶媒 2
実験手順
Ethyl6-benzyloxy-1-(tetrahydro-2H-pyran-2-yl)-indazole-3-carboxylate (182 mg) which can be prepared according to the method described in Reference example 21, etc. was dissolved in dehydrated THF (4.78 mL; manufactured by Kanto Chemical Co., Inc.). After the replacement with nitrogen, LiAlH4 (54 mg) was added at 0° C., and the mixture was stirred for 1 hour while warming to room temperature. After cooling to 0° C., THF/water=1/1(5 mL), rochelle salt (manufactured by Kanto Chemical Co., Inc.), and saturated aqueous solution of sodium hydrogen carbonate were added, and extraction was carried out twice with ethyl acetate. The organic layer was washed twice with water and once with brine and dried over anhydrous sodium sulfate. After the solvent was evaporated under reduced pressure, hexane was added to the residue and the solvent was evaporated under reduced pressure to give the title compound (155 mg).
後処理
- temperatureAfter cooling to 0° C.
- extractionextraction
- washThe organic layer was washed twice with water and once with brine
- dry with materialdried over anhydrous sodium sulfate
- customAfter the solvent was evaporated under reduced pressure, hexane
- additionwas added to the residue
- customthe solvent was evaporated under reduced pressure
出典と根拠
- ORDレコード
- ord-ec83bf7d67c346829a1e12a215131f79
- 出典データセット
- uspto-grants-2012_11
- 特許番号
- US08304443B2
反応ノート
読み込み中…