Toluene → tert-Butyl 4-(5-(hydroxymethyl)-[1,2,4]triazolo[4,3-a]pyrazin-8-yl)piperazine-1-carboxylate
反応式
[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][N:11]([C:14]2[C:15]3[N:16]([CH:24]=[N:25][N:26]=3)[C:17]([C:20](OC)=[O:21])=[CH:18][N:19]=2)[CH2:10][CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[H-].C([Al+]CC(C)C)C(C)C.C1(C)C=CC=CC=1>C(Cl)Cl>[OH:21][CH2:20][C:17]1[N:16]2[CH:24]=[N:25][N:26]=[C:15]2[C:14]([N:11]2[CH2:12][CH2:13][N:8]([C:6]([O:5][C:1]([CH3:4])([CH3:3])[CH3:2])=[O:7])[CH2:9][CH2:10]2)=[N:19][CH:18]=1参加物
反応物 3
生成物 1
試薬・触媒・溶媒 1
反応条件
- 温度
- -78 °C
実験手順
A 250 mL 3-necked round bottom flask was charged with methyl 8-(4-(tert-butoxycarbonyl)piperazin-1-yl)-[1,2,4]triazolo[4,3-a]pyrazine-5-carboxylate (3.0 g, 8.3 mmol) and dry CH2Cl2 (30 mL). To the above was added dropwise a solution of 1.5 M diisobutylaluminum hydride in toluene (11 mL, 16.5 mmol) at −78° C. The resulting mixture was stirred at −78° C. for further 1 h then quenched by slow addition of methanol (10 mL). The mixture was poured into saturated aqueous NH4Cl (200 mL) and extracted with ethyl ether (100 mL×2). The combined organic layers were washed with saturated aqueous NaHCO3 (100 mL) and brine (100 mL), dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was further purified by flash column chromatography on silica gel with 3% MeOH in CH2Cl2, to afford 1.4 g (50%) of the product as a white solid. MS m/z: 335 (M+H+).
後処理
- customthen quenched by slow addition of methanol (10 mL)
- additionThe mixture was poured into saturated aqueous NH4Cl (200 mL)
- extractionextracted with ethyl ether (100 mL×2)
- washThe combined organic layers were washed with saturated aqueous NaHCO3 (100 mL) and brine (100 mL)
- dry with materialdried over anhydrous Na2SO4
- concentrationconcentrated in vacuo
- customThe residue was further purified by flash column chromatography on silica gel with 3% MeOH in CH2Cl2
出典と根拠
- ORDレコード
- ord-f7d1f37fa1aa454c81b29a4c403fca61
- 出典データセット
- uspto-grants-2013_10
- 特許番号
- US08569300B2
反応ノート
読み込み中…