Diethyl Ether → 1-{3-[1-(1H-benzoimidazole-2-carbonyl)-azetidin-3-yl]-pyrazin-2-yl}-piperidin-4-one
反応式
[NH:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[C:2]1[C:10]([N:12]1[CH2:15][CH:14]([C:16]2[C:21]([N:22]3[CH2:27][CH2:26][CH:25]([OH:28])[CH2:24][CH2:23]3)=[N:20][CH:19]=[CH:18][N:17]=2)[CH2:13]1)=[O:11].CC(OI1(OC(C)=O)(OC(C)=O)OC(=O)C2C=CC=CC1=2)=O.CCOCC.CCOC(C)=O>C(Cl)Cl>[NH:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[C:2]1[C:10]([N:12]1[CH2:13][CH:14]([C:16]2[C:21]([N:22]3[CH2:27][CH2:26][C:25](=[O:28])[CH2:24][CH2:23]3)=[N:20][CH:19]=[CH:18][N:17]=2)[CH2:15]1)=[O:11]参加物
6
反応物 4
生成物 1
試薬・触媒・溶媒 1
実験手順
(1H-Benzoimidazol-2-yl)-{3-[3-(4-hydroxy-piperidin-1-yl)-pyrazin-2-yl]-azetidin-1-yl}-methanone (0.16 g, 0.42 mmol) was dissolved in anhydrous CH2Cl2 (20 mL), treated with Dess-Martin Periodinane (DMP) (195 mg, 0.46 mmol, 1.1 equiv) and stirred at RT until complete conversion controlled by TLC (Petro ether:EtOAc=1:1). The organic layer was washed with an aqueous solution of NaHCO3/Na2S2O3 (3×10 mL)), dried over Na2SO4, filtered and evaporated. The resulting residue was purified by flash chromatography (20% to 40% EtOAc in petroleum ether) to give 1-{3-[1-(1H-benzoimidazole-2-carbonyl)-azetidin-3-yl]-pyrazin-2-yl}-piperidin-4-one (0.134 g, 0.36 mmol, 85% yield) as a white solid.
後処理
- washThe organic layer was washed with an aqueous solution of NaHCO3/Na2S2O3 (3×10 mL)),
- dry with materialdried over Na2SO4
- filtrationfiltered
- customevaporated
- customThe resulting residue was purified by flash chromatography (20% to 40% EtOAc in petroleum ether)
出典と根拠
- ORDレコード
- ord-6ca89c4be05841cf9f23fe8bf104b241
- 出典データセット
- uspto-grants-2015_02
- 特許番号
- US08957073B2
反応ノート
読み込み中…