Methyl chloroformate → 7-(tert-Butyl) 5-Methyl (6S,7S)-6-(4-Phenylpiperazine-1-carbonyl)-5-azaspiro[2.5]octane-5,7-dicarboxylate
反応式
Cl[C:2]([O:4][CH3:5])=[O:3].[C:6]1([N:12]2[CH2:17][CH2:16][N:15]([C:18]([C@@H:20]3[C@@H:27]([C:28]([O:30][C:31]([CH3:34])([CH3:33])[CH3:32])=[O:29])[CH2:26][C:23]4([CH2:25][CH2:24]4)[CH2:22][NH:21]3)=[O:19])[CH2:14][CH2:13]2)[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1.C(N(C(C)C)CC)(C)C>C(#N)C.C(OCC)C>[C:6]1([N:12]2[CH2:13][CH2:14][N:15]([C:18]([C@@H:20]3[C@@H:27]([C:28]([O:30][C:31]([CH3:34])([CH3:33])[CH3:32])=[O:29])[CH2:26][C:23]4([CH2:24][CH2:25]4)[CH2:22][N:21]3[C:2]([O:4][CH3:5])=[O:3])=[O:19])[CH2:16][CH2:17]2)[CH:7]=[CH:8][CH:9]=[CH:10][CH:11]=1参加物
6
反応物 3
生成物 1
試薬・触媒・溶媒 2
実験手順
Methyl chloroformate (55 μL, 700 μL) was added to a solution of tert-butyl(6S,7S)-6-[(4-phenylpiperazin-1-yl)carbonyl]-5-azaspiro[2.5]octane-7-carboxylate (248.4 mg, 0.62 mmol) and di-isopropylethylamine (0.70 mmol, 0.125 mL) in 5 mL acetonitrile. The mixture was stirred at RT for 3 h. Solvent was removed to afford a residue which was dissolved in ethyl ether (15 mL), washed with water (3×2 mL) and dried over Na2SO4. The solution was filtered and concentrated to afford 281 mg of the 7-tert-butyl 5-methyl(6S,7S)-6-[(4-phenylpiperazin-1-yl)carbonyl]-5-azaspiro[2.5]octane-5,7-dicarboxylate.
後処理
- customSolvent was removed
- customto afford a residue which
- washwashed with water (3×2 mL)
- dry with materialdried over Na2SO4
- filtrationThe solution was filtered
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-69580a52110647b295135762eab871ed
- 出典データセット
- uspto-grants-2016_08
- 特許番号
- US09403775B2
反応ノート
読み込み中…