(3R)-3-ethyl-7-fluoro-4-(4-hydroxybenzoyl)-1-methyl-3,4-dihydroquinoxalin-2(1H)-one → (3R)-3-ethyl-6-fluoro-4-(4-hydroxybenzoyl)-1-isobutyl-3,4-dihydroquinoxalin-2(1H)-one
反応式
[CH2:1]([C@H:3]1[N:12]([C:13](=[O:22])[C:14]2[CH:19]=[CH:18][C:17]([O:20]C)=[CH:16][CH:15]=2)[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([F:23])[CH:10]=2)[N:5]([CH2:24][CH:25]([CH3:27])[CH3:26])[C:4]1=[O:28])[CH3:2].C([C@H]1N(C(=O)C2C=CC(O)=CC=2)C2C(=CC(F)=CC=2)N(C)C1=O)C>>[CH2:1]([C@H:3]1[N:12]([C:13](=[O:22])[C:14]2[CH:19]=[CH:18][C:17]([OH:20])=[CH:16][CH:15]=2)[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([F:23])[CH:10]=2)[N:5]([CH2:24][CH:25]([CH3:27])[CH3:26])[C:4]1=[O:28])[CH3:2]参加物
3
反応物 2
生成物 1
実験手順
(3R)-3-Ethyl-6-fluoro-4-(4-methoxybenzoyl)-1-isobutyl-3,4-dihydroquinoxalin-2(1H)-one was treated according to the procedure for the preparation of (3R)-3-ethyl-7-fluoro-4-(4-hydroxybenzoyl)-1-methyl-3,4-dihydroquinoxalin-2(1H)-one (see Example 1) to yield (3R)-3-ethyl-6-fluoro-4-(4-hydroxybenzoyl)-1-isobutyl-3,4-dihydroquinoxalin-2(1H)-one (93%). [α]D25=−272° (c=0.010 G/ML, CHCl3); MS (ESI) m/z 371 ([M+H]+); MS (ESI) m/z 369 ([M−H]−); HRMS: calcd for C21H23FN2O3, 370.1693; found (ESI_FT), 371.17594; Anal. Calcd for C21H23FN2O3: C, 68.09; H, 6.26; N, 7.56. Found: C, 67.85; H, 6.24; N, 7.65.