1,1'-Biphenyl-4-yl-boronic acid → 1-(4(S)-benzyl-2,2-dimethyl-oxazolidinyl)-2-(4-biphenyl4-yl-pyrazol-1-yl)-ethanone
반응식
[C:1]1([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[CH:6]=[CH:5][C:4]([C:7]2[CH:11]=CO[CH:8]=2)=[CH:3][CH:2]=1.[CH2:18]([C@H:25]1[CH2:29][O:28][C:27]([CH3:31])([CH3:30])[N:26]1[C:32](=[O:40])[CH2:33][N:34]1C=C(I)C=[N:35]1)[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1.C1(C2C=CC=CC=2)C=CC(B(O)O)=CC=1>>[CH2:18]([C@H:25]1[CH2:29][O:28][C:27]([CH3:31])([CH3:30])[N:26]1[C:32](=[O:40])[CH2:33][N:34]1[CH:8]=[C:7]([C:4]2[CH:3]=[CH:2][C:1]([C:12]3[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=3)=[CH:6][CH:5]=2)[CH:11]=[N:35]1)[C:19]1[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=1참가 물질
4
실험 절차
According to the procedure described in Example 1(a) for the preparation of 3-biphenyl-4-yl-furan, 1-(4(S)-benzyl-2,2-dimethyl-oxazolidinyl)-2-(4-iodopyrazol-1-yl)-ethanone was coupled to 4-biphenylboronic acid to provide in 39% yield 1-(4(S)-benzyl-2,2-dimethyl-oxazolidinyl)-2-(4-biphenyl-4-yl-pyrazol-1-yl)-ethanone as a white solid, mp 150-1° C.