3-Cyano-5-(pentafluoro-lambda6-sulphanyl)benzoic acid → 3-Cyano-N-(3-{6-[1-(4-methoxybenzyl)-1H-pyrazol-4-yl]-1H-imidazo[1,2-b]pyrazol-1-yl}-4-methylphenyl)-5-(pentafluoro-lambda6-sulphanyl)benzamide
반응식
[CH3:1][O:2][C:3]1[CH:30]=[CH:29][C:6]([CH2:7][N:8]2[CH:12]=[C:11]([C:13]3[CH:14]=[C:15]4[N:20]([C:21]5[CH:22]=[C:23]([CH:25]=[CH:26][C:27]=5[CH3:28])[NH2:24])[CH:19]=[CH:18][N:16]4[N:17]=3)[CH:10]=[N:9]2)=[CH:5][CH:4]=1.[C:31]([C:33]1[CH:34]=[C:35]([CH:39]=[C:40]([S:42]([F:47])([F:46])([F:45])([F:44])[F:43])[CH:41]=1)[C:36](O)=[O:37])#[N:32]>>[C:31]([C:33]1[CH:34]=[C:35]([CH:39]=[C:40]([S:42]([F:46])([F:47])([F:43])([F:44])[F:45])[CH:41]=1)[C:36]([NH:24][C:23]1[CH:25]=[CH:26][C:27]([CH3:28])=[C:21]([N:20]2[C:15]3[N:16]([N:17]=[C:13]([C:11]4[CH:10]=[N:9][N:8]([CH2:7][C:6]5[CH:5]=[CH:4][C:3]([O:2][CH3:1])=[CH:30][CH:29]=5)[CH:12]=4)[CH:14]=3)[CH:18]=[CH:19]2)[CH:22]=1)=[O:37])#[N:32]참가 물질
3
반응물 2
생성물 1
실험 절차
80 mg (0.16 mmol) of the compound of Example 60A and 66 mg (0.24 mmol) of the compound of Example 23A were reacted with one another analogously to Example 48A. In deviation from the work-up described therein, here, the mixture was separated directly into its components by preparative HPLC (Method 21). The product-containing fractions were concentrated under reduced pressure and the residue was dried under high vacuum. This gave 84 mg (64% of theory, 80% pure) of the title compound.
후처리
- customhere, the mixture was separated directly into its components by preparative HPLC (Method 21)
- concentrationThe product-containing fractions were concentrated under reduced pressure
- customthe residue was dried under high vacuum
출처 및 근거
- ORD 기록
- ord-62509c420c4342d18528512d93d1e75c
- 출처 데이터셋
- uspto-grants-2016_07
- 특허 번호
- US09394309B2
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