반응식
[CH3:1][O:2][C:3]1[CH:8]=[C:7](B2OC(C)(C)C(C)(C)O2)[CH:6]=[CH:5][C:4]=1[NH:18][C:19]([C:21]1[N:25]([CH3:26])[C:24]2[S:27][CH:28]=[CH:29][C:23]=2[CH:22]=1)=[O:20].Br[C:31]1[N:32]=[C:33]([C@H:41]2[CH2:46][CH2:45][C@H:44]([N:47]3[CH2:52][CH2:51][N:50]([CH3:53])[CH2:49][CH2:48]3)[CH2:43][CH2:42]2)[N:34]2[CH:39]=[CH:38][N:37]=[C:36]([CH3:40])[C:35]=12>>[CH3:1][O:2][C:3]1[CH:8]=[C:7]([C:31]2[N:32]=[C:33]([C@H:41]3[CH2:42][CH2:43][C@H:44]([N:47]4[CH2:48][CH2:49][N:50]([CH3:53])[CH2:51][CH2:52]4)[CH2:45][CH2:46]3)[N:34]3[CH:39]=[CH:38][N:37]=[C:36]([CH3:40])[C:35]=23)[CH:6]=[CH:5][C:4]=1[NH:18][C:19]([C:21]1[N:25]([CH3:26])[C:24]2[S:27][CH:28]=[CH:29][C:23]=2[CH:22]=1)=[O:20]참가 물질
3
실험 절차
Reaction of N-(2-methoxy-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-6-methyl-6H-thieno[2,3-b]pyrrole-5-carboxamide (32 mg) and 1-bromo-8-methyl-3-((trans)-4-(4-methylpiperazin-1-yl)cyclohexyl)imidazo[1,5-a]pyrazine (30 mg) according to the procedure described in example 4 step 4c and purification by column chromatography (silica gel; dichloromethane with gradient 0 to 20% of methanol) gave N-(2-methoxy-4-(8-methyl-3-((trans)-4-(4-methylpiperazin-1-yl)cyclohexyl)imidazo[1,5-a]pyrazin-1-yl)phenyl)-6-methyl-6H-thieno[2,3-b]pyrrole-5-carboxamide (13 mg)
후처리
- customdescribed in example 4 step 4c and purification by column chromatography (silica gel; dichloromethane with gradient 0 to 20% of methanol)
출처 및 근거
- ORD 기록
- ord-6e97c52d86d748feae76aff460e3b1bc
- 출처 데이터셋
- uspto-grants-2014_02
- 특허 번호
- US08658794B2
연결된 노트
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