1-(4-Fluorophenyl)piperazine → 3-(2-(4-(4-fluorophenyl)piperazin-1-yl)ethyl)-4,5,6,7-tetrahydro-2H-indazole
반응식
[F:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[CH2:13][CH2:12][NH:11][CH2:10][CH2:9]2)=[CH:4][CH:3]=1.[N:14]1[NH:15][C:16]([CH2:23][CH2:24]C(O)=O)=[C:17]2[C:22]=1[CH2:21][CH2:20][CH2:19][CH2:18]2.ClC1C=CC(C2CCNCC2)=CC=1>>[F:1][C:2]1[CH:3]=[CH:4][C:5]([N:8]2[CH2:13][CH2:12][N:11]([CH2:24][CH2:23][C:16]3[NH:15][N:14]=[C:22]4[C:17]=3[CH2:18][CH2:19][CH2:20][CH2:21]4)[CH2:10][CH2:9]2)=[CH:6][CH:7]=1참가 물질
4
실험 절차
In the same manner as in Example 102 except that 2-(4,5,6,7-tetrahydro-2H-indazol-3-yl)acetic acid obtained in Starting Material Synthesis Example 2 and 1-(4-fluorophenyl)piperazine were used instead of 3-(4,5,6,7-tetrahydro-2H-indazol-3-yl)propionic acid obtained in Staring Material Synthesis Example 1 and 4-(4-chlorophenyl)piperidine, 3-(2-(4-(4-fluorophenyl)piperazin-1-yl)ethyl)-4,5,6,7-tetrahydro-2H-indazole is obtained.