반응식
Br[C:2]1[C:10]2[C:9]([Cl:11])=[N:8][CH:7]=[N:6][C:5]=2[NH:4][CH:3]=1.[Li]CCCC.[CH3:17][Sn:18](Cl)([CH3:20])[CH3:19].[Cl-].[NH4+]>C1COCC1>[CH3:17][Sn:18]([CH3:20])([CH3:19])[C:2]1[C:10]2[C:9]([Cl:11])=[N:8][CH:7]=[N:6][C:5]=2[NH:4][CH:3]=1참가 물질
6
반응 조건
- 온도
- -78 °C
실험 절차
To a solution of the compound from Step A (0.92 g, 4 mmol) in THF (25 mL) was added n-BuLi (2.5 M solution in hexane, 3.48 mL) dropwise at −78° C. After the addition, the reaction mixture was stirred at −78° C. for an additional 30 min. To this solution was added trimethyltin chloride (0.88 g, 4.4 mmol) in THF (8 mL) dropwise for a period of 10 min. The reaction mixture was brought to room temperature slowly and stirred at room temperature overnight. Saturated aqueous ammonium chloride (60 mL) was added and extracted with ethyl acetate (3×70 mL). The combined organic extracts were washed with brine, dried over Na2SO4 and evaporated to dryness. The residue was purified over silica gel to give the title compound as a colorless solid.
후처리
- additionAfter the addition
- customwas brought to room temperature
- stirringstirred at room temperature overnight
- extractionextracted with ethyl acetate (3×70 mL)
- washThe combined organic extracts were washed with brine
- dry with materialdried over Na2SO4
- customevaporated to dryness
- customThe residue was purified over silica gel
출처 및 근거
- ORD 기록
- ord-3a54b8808b9645c2a9df29a1b12740b8
- 출처 데이터셋
- uspto-grants-2008_01
- 특허 번호
- US07323453B2
연결된 노트
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