Ethyl 4-[(5-{3-methyl-5-[(4-methylpyrimidin-2-yl)amino]phenyl}-1,3-thiazol-2-yl)methylidene]cyclohexanecarboxylate → Ethyl 4-[(5-{3-methyl-5-[(4-methylpyrimidin-2-yl)amino]phenyl}-1,3-thiazol-2-yl)methyl]cyclohexanecarboxylate
반응식
[CH3:1][C:2]1[CH:3]=[C:4]([C:16]2[S:20][C:19]([CH:21]=[C:22]3[CH2:27][CH2:26][CH:25]([C:28]([O:30][CH2:31][CH3:32])=[O:29])[CH2:24][CH2:23]3)=[N:18][CH:17]=2)[CH:5]=[C:6]([NH:8][C:9]2[N:14]=[C:13]([CH3:15])[CH:12]=[CH:11][N:10]=2)[CH:7]=1>C(O)C.[Pd]>[CH3:1][C:2]1[CH:3]=[C:4]([C:16]2[S:20][C:19]([CH2:21][CH:22]3[CH2:27][CH2:26][CH:25]([C:28]([O:30][CH2:31][CH3:32])=[O:29])[CH2:24][CH2:23]3)=[N:18][CH:17]=2)[CH:5]=[C:6]([NH:8][C:9]2[N:14]=[C:13]([CH3:15])[CH:12]=[CH:11][N:10]=2)[CH:7]=1참가 물질
4
반응물 1
생성물 1
시약·촉매·용매 2
실험 절차
Ethyl 4-[(5-{3-methyl-5-[(4-methylpyrimidin-2-yl)amino]phenyl}-1,3-thiazol-2-yl)methylidene]cyclohexanecarboxylate (175 mg, 0.390 mmol) was taken up in ethanol (5 mL), and palladium on carbon (10% loading, 104 mg, 0.098 mmol) was added. The reaction was purged with hydrogen gas (3×) and stirred under a hydrogen atmosphere (via balloon) overnight at room temperature. The mixture was then filtered through CELITE, concentrated under reduced pressure, and the residue purified by flash chromatography on silica gel (0-50% ethyl acetate in hexanes) to provide ethyl 4-[(5-{3-methyl-5-[(4-methylpyrimidin-2-yl)amino]phenyl}-1,3-thiazol-2-yl)methyl]cyclohexanecarboxylate (yellow gum) as a 3:1 mixture of diastereomers. MS ESI calc'd. for C25H31N4O2S [M+H]+ 451. found 451. 1H NMR (500 MHz, DMSO-d6) δ 9.58 (s, 1H), 8.34 (d, J=5.0, 1H), 7.96 (s, 1H), 7.92 (s, 1H), 7.51 (s, 1H), 7.03 (s, 1H), 6.74 (d, J=5.0 Hz, 1H), 4.06 (q, J=7.1 Hz, 2H), 2.88 (d, J=7.3 Hz, 2H), 2.36 (s, 3H), 2.29 (s, 3H), 1.93-1.83 (m, 4H), 1.62-1.45 (m, 4H), 1.24 (d, J=9.5 Hz, 2H), 1.18-1.14 (m, 3H). rhSyk activity=++