反応式
[NH:1]1[CH2:5][CH2:4][C@@H:3]([NH:6]C(=O)OC(C)(C)C)[CH2:2]1.[F:14][CH2:15][C:16](=O)[CH2:17][F:18].C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+]>ClCCl>[F:14][CH2:15][CH:16]([N:1]1[CH2:5][CH2:4][C@@H:3]([NH2:6])[CH2:2]1)[CH2:17][F:18]参加物
5
実験手順
To a solution of (R)-tert-butyl pyrrolidin-3-ylcarbamate (0.500 g) and 1,3-difluoropropan-2-one (0.278 g) in dichloromethane (5 mL) was added sodium triacetoxyborohydride (0.853 g). After stirring for 1 hour, the reaction was quenched with saturated NaHCO3 solution (5 mL). The product was extracted into dichloromethane (25 mL), dried over magnesium sulfate, filtered, and concentrated. The resulting crude material was treated with HCl (4.0M in dioxane, 4 mL) and methanol (1 mL) and stirred for 1 hour. The mixture was concentrated to provide the title compound.
後処理
- customthe reaction was quenched with saturated NaHCO3 solution (5 mL)
- extractionThe product was extracted into dichloromethane (25 mL)
- dry with materialdried over magnesium sulfate
- filtrationfiltered
- concentrationconcentrated
- additionThe resulting crude material was treated with HCl (4.0M in dioxane, 4 mL) and methanol (1 mL)
- stirringstirred for 1 hour
- concentrationThe mixture was concentrated
出典と根拠
- ORDレコード
- ord-82df88e44f3a48f0965fc62a96934ead
- 出典データセット
- uspto-grants-2015_05
- 特許番号
- US09029404B2
関連ノート
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