반응식
C(O[C:4]([C:6]1[C:10]([CH3:11])=[C:9]([C:12]2[CH:17]=[CH:16][C:15]([Cl:18])=[CH:14][CH:13]=2)[N:8]([C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][C:20]=2[Cl:25])[N:7]=1)=[O:5])C.[CH2:26]([O:28][C:29]([C:31]1([C:37]2[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=2)[CH2:36][CH2:35][NH:34][CH2:33][CH2:32]1)=[O:30])[CH3:27].ClC1C=CC(C2N(C3C=CC=CC=3Cl)N=C(C(N3CCN(C4C=CC=CC=4)CC3)=O)C=2CC#N)=CC=1>>[CH2:26]([O:28][C:29]([C:31]1([C:37]2[CH:38]=[CH:39][CH:40]=[CH:41][CH:42]=2)[CH2:32][CH2:33][N:34]([C:4]([C:6]2[C:10]([CH3:11])=[C:9]([C:12]3[CH:17]=[CH:16][C:15]([Cl:18])=[CH:14][CH:13]=3)[N:8]([C:19]3[CH:24]=[CH:23][CH:22]=[CH:21][C:20]=3[Cl:25])[N:7]=2)=[O:5])[CH2:35][CH2:36]1)=[O:30])[CH3:27]참가 물질
4
반응물 3
생성물 1
실험 절차
The ester compound [A1] was hydrolysed according to the procedure for the last step in the synthesis of [1.1]. The resulting acid was coupled with 4-phenyl-piperidine-4-carboxylic acid ethyl ester according to the procedure for the synthesis of [C1] to give 1-[1-(2-chloro-phenyl)-5-(4-chloro-phenyl)-4-methyl-1H-pyrazole-3-carbonyl]-4-phenyl-piperidine-4-carboxylic acid ethyl ester.
출처 및 근거
- ORD 기록
- ord-cc46028c9688454bb90018034e64b995
- 출처 데이터셋
- uspto-grants-2012_04
- 특허 번호
- US08148404B2
연결된 노트
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