Diethyl (formylamino)(8-quinolinylmethyl)malonate → ethyl 2,3,6,7-tetrahydro-3-oxo-2-(formylamino)-1H,5H-benzo(ij)quinolizine-2-carboxylate
反応式
[CH:1]([NH:3][C:4]([CH2:15][C:16]1[CH:17]=[CH:18][CH:19]=[C:20]2[C:25]=1[N:24]=[CH:23][CH:22]=[CH:21]2)([C:10](OCC)=[O:11])[C:5]([O:7][CH2:8][CH3:9])=[O:6])=[O:2].[H][H]>C(O)(=O)C.[Pt]=O>[O:11]=[C:10]1[C:4]([NH:3][CH:1]=[O:2])([C:5]([O:7][CH2:8][CH3:9])=[O:6])[CH2:15][C:16]2=[CH:17][CH:18]=[CH:19][C:20]3=[C:25]2[N:24]1[CH2:23][CH2:22][CH2:21]3参加物
実験手順
A mixture of diethyl (formylamino)(8-quinolinylmethyl)malonate (9.2 g, 26.7 mmol) and platinum oxide (0.7 g) in glacial acetic acid (150 mL) was hydrogenated (50 lb initial pressure) for 15 minutes (hydrogen uptake ca. 2 equiv). The mixture was filtered through celite and the solvent removed under reduced pressure. The product was partitioned between ethyl acetate and sodium hydroxide solution. The ethyl acetate phase was washed with water, the ethyl acetate was evaporated, and the product was crystallized from ether to give 7.8 g (97%) of ethyl 2,3,6,7-tetrahydro-3-oxo-2-(formylamino)- 1H,5H-benzo(ij)quinolizine-2-carboxylate, mp 103°-106° C. Anal. Calc'd for C16H18N2O4 : C, 63.56; H, 6.00; N, 9.27. Found: C, 63.51; H, 6.09; N, 9.18.
後処理
- customfor 15 minutes
- filtrationThe mixture was filtered through celite
- customthe solvent removed under reduced pressure
- customThe product was partitioned between ethyl acetate and sodium hydroxide solution
- washThe ethyl acetate phase was washed with water
- customthe ethyl acetate was evaporated
- customthe product was crystallized from ether
出典と根拠
- ORDレコード
- ord-7eff329947704dc0a297d998208b65f6
- 出典データセット
- uspto-grants-1995_07
- 特許番号
- US05436240
反応ノート
読み込み中…