Dabco → Methyl 6-(3,3-diethoxyprop-1-ynyl)-5-methyl-3-oxo-4-(3-(trifluoromethyl)phenyl)-3,4-dihydropyrazine-2-carboxylate
반응식
I[C:2]1[N:7]=[C:6]([C:8]([O:10][CH3:11])=[O:9])[C:5](=[O:12])[N:4]([C:13]2[CH:18]=[CH:17][CH:16]=[C:15]([C:19]([F:22])([F:21])[F:20])[CH:14]=2)[C:3]=1[CH3:23].C(P(C(C)(C)C)C(C)(C)C)(C)(C)C.[CH2:37]([O:39][CH:40]([O:43][CH2:44][CH3:45])[C:41]#[CH:42])[CH3:38].N12CCN(CC1)CC2>CCCCCC.CN(C=O)C.[CH2-]C=C.[CH2-]C=C.Cl[Pd+].Cl[Pd+]>[CH2:37]([O:39][CH:40]([O:43][CH2:44][CH3:45])[C:41]#[C:42][C:2]1[N:7]=[C:6]([C:8]([O:10][CH3:11])=[O:9])[C:5](=[O:12])[N:4]([C:13]2[CH:18]=[CH:17][CH:16]=[C:15]([C:19]([F:22])([F:21])[F:20])[CH:14]=2)[C:3]=1[CH3:23])[CH3:38]참가 물질
반응물 4
생성물 1
시약·촉매·용매 3
실험 절차
Methyl 6-iodo-5-methyl-3-oxo-4-[3-(trifluoromethyl)phenyl]-3,4-dihydropyrazine-2-carboxylate (1.2 g, 2.8 mmol), allylpalladium(II)chloride dimer (0.0072 g), 10% by weight tri(tert-butyl)phosphine in hexane (2.1 mL) and anhydrous DMF (3.0 mL) were stirred until a clear solution was obtained. Propargylaldehyde diethyl acetal (0.44 mL, 3.1 mmol) in anhydrous DMF (2.3 mL) was added, followed by 1,4-diazabicyclo[2.2.2]octane (0.63 g, 5.6 mmol) in small portions. The red solution was purged with dry argon for 5 minutes and then stirred under argon at RT. After 4 h, the solvent was evaporated using an oil pump. The residue was taken up in acetonitrile (10 mL), filtered through glass-wool and then concentrated with silica. Chromatography on silica with ethyl acetate-heptanes (1:10 and 1:2) as eluents gave 0.46 g (37%) of the title compound as a yellow oil.
후처리
- customwas obtained
- customThe red solution was purged with dry argon for 5 minutes
- customthe solvent was evaporated
- filtrationfiltered through glass-wool
- concentrationconcentrated with silica
출처 및 근거
- ORD 기록
- ord-6a4355a2a95843e88a8d263954a32752
- 출처 데이터셋
- uspto-grants-2013_04
- 특허 번호
- US08410114B2
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