反応式
[C:1](O[BH-](OC(=O)C)OC(=O)C)(=O)[CH3:2].[Na+].C(O)(=O)C.[C:19]([N:26]1C=CC(C=O)=[C:28]([NH2:34])[CH2:27]1)([O:21][C:22]([CH3:25])([CH3:24])[CH3:23])=[O:20].[NH2:35][CH:36]1[CH2:41][CH2:40][N:39]([C:42]([O:44][CH2:45][CH3:46])=[O:43])[CH2:38][CH2:37]1.Cl[CH:48](Cl)[CH3:49]>>[C:22]([O:21][C:19]([NH:26][C:27]1[CH:28]=[N:34][CH:1]=[CH:2][C:48]=1[CH2:49][NH:35][CH:36]1[CH2:37][CH2:38][N:39]([C:42]([O:44][CH2:45][CH3:46])=[O:43])[CH2:40][CH2:41]1)=[O:20])([CH3:23])([CH3:24])[CH3:25]参加物
6
反応物 5
生成物 1
実験手順
Sodium triacetoxyborohydride (0.57 g, 2.70 mmol) and acetic acid (0.41, 6.75 mmol) were added to a solution of N-Boc-3-amino-4-pyridine carboxaldehyde (0.50 g, 2.25 mmol) and ethyl 4-aminopiperidine-1-carboxylate (0.47 g, 2.70 mmol) in dichloroethane (5 mL) at room temperature. The reaction was stirred overnight, and quenched with saturated aqueous sodium bicarbonate. This was separated, extracted with ethyl acetate and the combined organics were dried over sodium sulfate. The solution was filtered and evaporated to give the crude product. This was purified by chromatography (silica gel, 1 to 12% methanol in methylene chloride gradient elution), which gave the title compound (0.47 g). MS 379.3.
後処理
- customquenched with saturated aqueous sodium bicarbonate
- customThis was separated
- extractionextracted with ethyl acetate
- dry with materialthe combined organics were dried over sodium sulfate
- filtrationThe solution was filtered
- customevaporated
- customto give the crude product
- customThis was purified by chromatography (silica gel, 1 to 12% methanol in methylene chloride gradient elution), which
出典と根拠
- ORDレコード
- ord-7597ef02e405429a8d0c1fafb8776021
- 出典データセット
- uspto-grants-2010_08
- 特許番号
- US07772224B2
関連ノート
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