Acetic Acid → 4-Phenyl-5,6-dihydro-4H-imidazo[4,5,1-ij]quinolin-2(1H)-one

反応式

CO[N:3]1[C:13]2=[C:14]3[C:9](=[CH:10][CH:11]=[CH:12]2)[CH2:8][CH2:7][CH:6]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[N:5]3[C:4]1=[O:21].C(O)C.C(O)(=O)C>>[C:15]1([CH:6]2[CH2:7][CH2:8][C:9]3[C:14]4=[C:13]([NH:3][C:4](=[O:21])[N:5]24)[CH:12]=[CH:11][CH:10]=3)[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=1

参加物

反応物 3

HCID 176Acetic Acid

HCID 702Ethanol

HCID 904095351-Methoxy-4-phenyl-5,6-dihydro-4H-imidazo[4,5,1-ij]quinolin-2(1H)-one

生成物 1

HCID 904094724-Phenyl-5,6-dihydro-4H-imidazo[4,5,1-ij]quinolin-2(1H)-one収率 85%

実験手順

A suspension of 1-methoxy-4-phenyl-5,6-dihydro-4H-imidazo[4,5,1-ij]quinolin-2(1H)-one (0.575 g, 2.05 mmol) in ethanol (35.9 mL, 615 mmol) was heated to dissolve residual solids and the resulting solution was cooled to room temperature. The solution was treated with acetic acid (0.233 mL, 4.10 mmol), degassed with nitrogen, treated with palladium catalyst (0.575 g, 100 wt %) (10% Pd on carbon, Degussa type) and hydrogenated for 17 h. The reaction mixture was filtered and the catalyst was washed with ethanol and methanol. The filtrate was then concentrated to give the desired product (0.436 g, 85%) as a racemic mixture that was used without further purification. LCMS calculated for C16H15N2O (M+H)+: m/z=251.1. found: 251.1.