反応式
F[C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][C:9]=1[N+:10]([O-:12])=[O:11])[C:5]#[N:6].[C:13]1([C@@H:19]2[C@@H:23]([C:24]3[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=3)[O:22][C:21]3([CH2:34][CH2:33][CH2:32][C@H:31]([CH2:35][NH2:36])[CH2:30]3)[O:20]2)[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1.C(=O)([O-])[O-].[K+].[K+].C(Cl)Cl>C(#N)C.CO>[C:13]1([C@@H:19]2[C@@H:23]([C:24]3[CH:25]=[CH:26][CH:27]=[CH:28][CH:29]=3)[O:22][C:21]3([CH2:34][CH2:33][CH2:32][C@H:31]([CH2:35][NH:36][C:2]4[CH:3]=[C:4]([CH:7]=[CH:8][C:9]=4[N+:10]([O-:12])=[O:11])[C:5]#[N:6])[CH2:30]3)[O:20]2)[CH:14]=[CH:15][CH:16]=[CH:17][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
A mixture of 3-fluoro-4-nitrobenzonitrile (55.5 g, 334 mmol), 1-[(2R,3R,7S)-2,3-diphenyl-1,4-dioxaspiro[4.5]dec-7-yl]methanamine (103 g, 318 mmol) and potassium carbonate (88 g, 637 mmol) in acetonitrile (2654 mL) was stirred at RT for 5 days (˜200 mL DCM was added to help with solubility). The resulting solution was filtered and the solids washed with MeCN. The resulting solution was concentrated to give the crude product that was dissolved in MeOH (500 mL) and allowed to crystallize with stirring. The slurry was allowed to stir at RT overnight, filtered and the solids dried under reduced pressure to give 3-({[(2R,3R,7S)-2,3-diphenyl-1,4-dioxaspiro[4.5]dec-7-yl]methyl}amino)-4-nitrobenzonitrile (131.41 g, 88% yield). The product was used without further purification.
後処理
- filtrationThe resulting solution was filtered
- washthe solids washed with MeCN
- concentrationThe resulting solution was concentrated
- customto give the crude product that
- customto crystallize
- stirringwith stirring
- stirringto stir at RT overnight
- filtrationfiltered
- customthe solids dried under reduced pressure
出典と根拠
- ORDレコード
- ord-487b7f2e91fd435589bbee19d4572d21
- 出典データセット
- uspto-grants-2015_11
- 特許番号
- US09187464B2
関連ノート
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