반응식
[NH2:1][C:2]1[N:7]=[C:6]([CH3:8])[C:5](Br)=[CH:4][CH:3]=1.[CH3:10][Si:11]([C:14]#[CH:15])([CH3:13])[CH3:12].O1CCOCC1.O>[Cu]I.C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.Cl[Pd]Cl.C(OCC)(=O)C>[CH3:8][C:6]1[N:7]=[C:2]([NH2:1])[CH:3]=[CH:4][C:5]=1[C:15]#[C:14][Si:11]([CH3:13])([CH3:12])[CH3:10]참가 물질
반응물 4
생성물 1
시약·촉매·용매 3
반응 조건
- 온도
- 100 °C
실험 절차
To a mixture of 6-amino-3-bromo-2-methylpyridine (200 mg, 1.0 mmol), trimethylsilylacetylene (0.22 mL, 1.6 mmol), copper (I) iodide (9.9 mg, 0.052 mmol), and 1,4-dioxane (1.5 mL) was added bis(triphenylphosphine)palladium (II) chloride (73 mg, 0.10 mmol), which was stirred under nitrogen atmosphere for 3 hours and 30 minutes at 100° C. The reaction mixture was allowed to room temperature, water was added to the reaction mixture at the same temperature, ethyl acetate was added, and the mixture was filtered through a Celite pad. The organic layer of the filtrate was separated and washed with saturated aqueous sodium chloride, and was concentrated under a reduced pressure, and the residue thus obtained was purified by silica gel column chromatography (heptane:ethyl acetate=2:1) to obtain the title compound (140 mg, 57%, purity: 86%).
후처리
- customwas allowed to room temperature
- additionwas added
- filtrationthe mixture was filtered through a Celite pad
- customThe organic layer of the filtrate was separated
- washwashed with saturated aqueous sodium chloride
- concentrationwas concentrated under a reduced pressure
- customthe residue thus obtained
- customwas purified by silica gel column chromatography (heptane:ethyl acetate=2:1)
출처 및 근거
- ORD 기록
- ord-4a4737664898482ca5c07efeed9c36d1
- 출처 데이터셋
- uspto-grants-2010_04
- 특허 번호
- US07691882B2
연결된 노트
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