Acetamidomalonic acid diethyl ester → HCID 67246761、化合物
反応式
[H-].[Na+].[C:3]([NH:6][CH:7]([C:13]([O:15][CH2:16][CH3:17])=[O:14])[C:8]([O:10][CH2:11][CH3:12])=[O:9])(=[O:5])[CH3:4].Br[CH:19]1[CH2:27][C:26]2[C:21](=[CH:22][CH:23]=[C:24]([CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH3:35])[CH:25]=2)[C:20]1=[O:36]>CN(C=O)C>[CH2:11]([O:10][C:8](=[O:9])[C:7]([NH:6][C:3](=[O:5])[CH3:4])([CH:19]1[CH2:27][C:26]2[C:21](=[CH:22][CH:23]=[C:24]([CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH3:35])[CH:25]=2)[C:20]1=[O:36])[C:13]([O:15][CH2:16][CH3:17])=[O:14])[CH3:12]参加物
5
実験手順
To a stirring solution of 60% NaH (1.194 g, 29.85 mmol) in DMF (5 mL) was added diethyl acetamidomalonate (6.484 g, 29.85 mmol) via cannula at 0° C. The solution was allowed to stir for 3 hours for anion to form. A solution of 3 (3.22 g, 9.95 mmol) in DMF (10 mL) was then added to then transferred to anion solution at 0° C. and left to stir over night at room temp. The reaction mixture was then poured over ice and extracted with EtOAc. The organic layer was washed with brine, dried with NaSO4 and concentrated. The product was then purified with silica gel chromatography eluding with 70% hexanes-30% EtOAc. The reaction provided 4 (2.842 g, 6.184 mmol, 65%).
後処理
- customto form
- customto then transferred to anion solution at 0° C.
- waitleft
- stirringto stir over night at room temp
- additionThe reaction mixture was then poured over ice
- extractionextracted with EtOAc
- washThe organic layer was washed with brine
- dry with materialdried with NaSO4
- concentrationconcentrated
- customThe product was then purified with silica gel chromatography
出典と根拠
- ORDレコード
- ord-c28649fa061e44d7a9d042c489596b51
- 出典データセット
- uspto-grants-2011_06
- 特許番号
- US07964649B2
反応ノート
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