methyl (2R)-2-amino-5-[5-[{2-[3,5-bis(trifluoromethyl)phenyl]-2-methylpropanoyl}(methyl)amino]-4-(4-fluoro-2-methylphenyl)-2-pyridinyl]-4-pentynoate → methyl (2R)-5-[5-[{2-[3,5-bis(trifluoromethyl)phenyl]-2-methylpropanoyl}(methyl)amino]-4-(4-fluoro-2-methylphenyl)-2-pyridinyl]-3,4-dihydro-2H-pyrrole-2-carboxylate
반응식
[NH2:1][C@H:2]([CH2:7][C:8]#[C:9][C:10]1[CH:15]=[C:14]([C:16]2[CH:21]=[CH:20][C:19]([F:22])=[CH:18][C:17]=2[CH3:23])[C:13]([N:24]([C:26](=[O:44])[C:27]([C:30]2[CH:35]=[C:34]([C:36]([F:39])([F:38])[F:37])[CH:33]=[C:32]([C:40]([F:43])([F:42])[F:41])[CH:31]=2)([CH3:29])[CH3:28])[CH3:25])=[CH:12][N:11]=1)[C:3]([O:5][CH3:6])=[O:4]>C(#N)C.FC(F)(F)S([O-])(=O)=O.[Ag+]>[F:37][C:36]([F:38])([F:39])[C:34]1[CH:35]=[C:30]([C:27]([CH3:28])([CH3:29])[C:26]([N:24]([CH3:25])[C:13]2[C:14]([C:16]3[CH:21]=[CH:20][C:19]([F:22])=[CH:18][C:17]=3[CH3:23])=[CH:15][C:10]([C:9]3[CH2:8][CH2:7][C@H:2]([C:3]([O:5][CH3:6])=[O:4])[N:1]=3)=[N:11][CH:12]=2)=[O:44])[CH:31]=[C:32]([C:40]([F:41])([F:43])[F:42])[CH:33]=1참가 물질
4
반응물 1
생성물 1
시약·촉매·용매 2
실험 절차
Silver trifluoromethanesulfonate (0.381 g, 1.483 mmol) was added portionwise to a solution of methyl (2R)-2-amino-5-[5-[{2-[3,5-bis(trifluoromethyl)phenyl]-2-methylpropanoyl}(methyl)amino]-4-(4-fluoro-2-methylphenyl)-2-pyridinyl]-4-pentynoate (Intermediate 13, 1.85 g, 2.97 mmol) in anhydrous Acetonitrile (25 ml) and the resulting reaction mixture was stirred at room temperature overnight. Volatiles were evaporated under vacuo at room temperature. The residue was taken-up in dichloromethane and filtered through a plug of celite to afford 2.2 g of the title compound as a brown solid (the material contained some residual acetonitrile, therefore overall recovered amount was higher than the theoretical amount).
후처리
- customthe resulting reaction mixture
- customVolatiles were evaporated under vacuo at room temperature
- filtrationfiltered through a plug of celite
출처 및 근거
- ORD 기록
- ord-0cb35fc63e4340b2ac368e0ac56b75f9
- 출처 데이터셋
- uspto-grants-2014_09
- 특허 번호
- US08822504B2
연결된 노트
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