Dimethylformamide → HCID 178474487, 화합물
반응식
C([N:4]1[C:8]([NH:9][C:10](=[O:12])[CH3:11])=[C:7](I)[C:6]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)=[N:5]1)(=O)C.[C:20]1([C:26]#[CH:27])[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1.C(N(CC)CC)C.CN(C=O)C>C(OCC)(=O)C.O.[Cu](I)I.Cl[Pd](Cl)([P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1>[C:14]1([C:6]2[C:7]([C:27]#[C:26][C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=3)=[C:8]([NH:9][C:10](=[O:12])[CH3:11])[NH:4][N:5]=2)[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=1참가 물질
9
반응 조건
- 온도
- 90 °C
실험 절차
Nitrogen was bubbled through a mixture of N-(2-acetyl-4-iodo-5-phenyl-pyrazol-3-yl)acetamide (31.87 g, 86.4 mmol), phenyl acetylene (17.6 g, 173 mmol), triethylamine (200 mL) and DMF (100 mL) for 15 min. Copper iodide (1.64 g, 8.6 mmol) and bis(triphenylphosphine)palladium(II) dichloride (3.0 g, 4.3 mmol) were added and the reaction mixture was stirred at 90° C. under nitrogen for 3 h. The reaction mixture was cooled to room temperature, diluted with ethyl acetate and water. The organic phase was washed with water and brine, dried (MgSO4), filtered and concentrated in vacuo. The residue was purified by column chromatography (silica gel, isohexane/ethyl acetate 5:1 to 1:1) yielding the title compound as a solid (12.5 g).
후처리
- temperatureThe reaction mixture was cooled to room temperature
- washThe organic phase was washed with water and brine
- dry with materialdried (MgSO4)
- filtrationfiltered
- concentrationconcentrated in vacuo
- customThe residue was purified by column chromatography (silica gel, isohexane/ethyl acetate 5:1 to 1:1)
출처 및 근거
- ORD 기록
- ord-e50406945cef4448ad379d3107464ae7
- 출처 데이터셋
- uspto-grants-2014_07
- 특허 번호
- US08765762B2
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