Hydrochloric Acid → diethyl 2-methyl-6b,9,10,10a-tetrahydro-1H-pyrido[3',4':4,5]pyrrolo[1,2,3-de]quinoxaline-3,8(2H,7H)-dicarboxylate
反応式
[CH3:1][CH:2]1[C:11](=O)[N:10]2[CH:13]3[CH2:18][CH2:17][N:16]([C:19]([O:21][CH2:22][CH3:23])=[O:20])[CH2:15][CH:14]3[C:8]3[C:9]2=[C:4]([CH:5]=[CH:6][CH:7]=3)[N:3]1[C:24]([O:26][CH2:27][CH3:28])=[O:25].Cl>C1COCC1.O>[CH3:1][CH:2]1[CH2:11][N:10]2[CH:13]3[CH2:18][CH2:17][N:16]([C:19]([O:21][CH2:22][CH3:23])=[O:20])[CH2:15][CH:14]3[C:8]3[C:9]2=[C:4]([CH:5]=[CH:6][CH:7]=3)[N:3]1[C:24]([O:26][CH2:27][CH3:28])=[O:25]参加物
5
反応物 2
生成物 1
試薬・触媒・溶媒 2
実験手順
To a solution of diethyl 2-methyl-1-oxo-6b,9,10,10a-tetrahydro-1H-pyrido[3′,4′:4,5]pyrrolo[1,2,3-de]quinoxaline-3,8(2H,7H)-dicarboxylate (300 mg, 0.77 mmol) in THF (10 mL) at rt was added BH3THF complex (3.8 mL, 3.8 mmol) and refluxed for 5 hours. At rt 6N HCl (10 mL) was added and stirred for 0.5 hour before the solution was diluted with water (20 mL), and extracted with EtOAc (2×20 mL). The combined extracts were dried over magnesium sulfate, concentrated, and purified by flash chromatography to afford diethyl 2-methyl-6b,9,10,10a-tetrahydro-1H-pyrido[3′,4′:4,5]pyrrolo[1,2,3-de]quinoxaline-3,8(2H,7H)-dicarboxylate (200 mg, 69%) as a clear oil. MS [M+H]+ 374.
後処理
- temperaturerefluxed for 5 hours
- extractionextracted with EtOAc (2×20 mL)
- dry with materialThe combined extracts were dried over magnesium sulfate
- concentrationconcentrated
- custompurified by flash chromatography
出典と根拠
- ORDレコード
- ord-ab4b82824bdb4de6a84a84f18f480357
- 出典データセット
- uspto-grants-2007_02
- 特許番号
- US07183282B2
反応ノート
読み込み中…