HCID 19853360、化合物 → HCID 19853335、化合物

反応式

C([O:8][C:9]1[C:10]([F:30])=[C:11]([F:29])[CH:12]=[C:13]2[C:18]=1[N:17]([NH:19][CH2:20][CH:21]=[O:22])[CH:16]=[C:15]([C:23]([O:25][CH2:26][CH3:27])=[O:24])[C:14]2=[O:28])C1C=CC=CC=1>C(Cl)(Cl)Cl.CO.[Pd]>[F:29][C:11]1[CH:12]=[C:13]2[C:18](=[C:9]([OH:8])[C:10]=1[F:30])[N:17]([NH:19][CH2:20][CH:21]=[O:22])[CH:16]=[C:15]([C:23]([O:25][CH2:26][CH3:27])=[O:24])[C:14]2=[O:28]

参加物

実験手順

Ethyl 8-benzyloxy-6,7-difluoro-1-(formylmethylamino)-4-oxo-1,4-dihydro-3-quinolinecarboxylate (330 mg) was hydrogenated over 5% Pd/C (50 mg) in chloroform (14 ml) for 4 hours. The reaction mixture was diluted with methanol (14 ml) and filtered. The filtered cake was washed with chloroform/methanol (1:1). The combined filtrate was evaporated and the residue was recrystallized from ethanol to give 239 mg of ethyl 6,7-difluoro-1-(formylmethylamino)-8-hydroxy-4-oxo-1,4-dihydro-3-quinolinecarboxylate, mp 221°-225° C. (dec.); MS m/z 326 (M+).