Sodium Iodide → 2-Ethyl-3-iodopyrazolo[1,5-a]pyridine
반응식
ClN1C(=O)CCC1=O.[CH2:9]([C:11]1[CH:19]=[C:14]2[CH:15]=[CH:16][CH:17]=[CH:18][N:13]2[N:12]=1)[CH3:10].[I-:20].[Na+]>C(OCC)(=O)C.O>[CH2:9]([C:11]1[C:19]([I:20])=[C:14]2[CH:15]=[CH:16][CH:17]=[CH:18][N:13]2[N:12]=1)[CH3:10]참가 물질
실험 절차
N-Chlorosuccinimide (411 g, 3.08 mol) was gradually added to a mixture of 2-ethylpyrazolo[1,5-a]pyridine (360 g, 2.46 mol), ethyl acetate (3600 mL), water (1800 mL) and sodium iodide (480 g, 3.20 mol, 1.3 equivalents) over a period of 30 minutes while cooling with ice, and then the reaction mixture was stirred for 2 hours and 20 minutes at room temperature. After the reaction, water and ethyl acetate were added to the reaction mixture and extraction was performed with ethyl acetate. The organic extract was washed twice with 10% aqueous sodium thiosulfate, and then concentrated. Hexane was added to the residue, the mixture was heated to dissolution and the resulting solution was filtered to remove insoluble residue. After then washing the hexane solution with water, the hexane layer was concentrated, the residue was dissolved in ethyl acetate and the solvent was evaporated to afford 663 g of the title compound (98.9% yield).
후처리
- temperaturewhile cooling with ice
- additionwere added to the reaction mixture and extraction
- extractionThe organic extract
- washwas washed twice with 10% aqueous sodium thiosulfate
- concentrationconcentrated
- additionHexane was added to the residue
- temperaturethe mixture was heated to dissolution
- filtrationthe resulting solution was filtered
- customto remove insoluble residue
- washAfter then washing the hexane solution with water
- concentrationthe hexane layer was concentrated
- dissolutionthe residue was dissolved in ethyl acetate
- customthe solvent was evaporated
출처 및 근거
- ORD 기록
- ord-c7dd837d22394699abfd808b14375e33
- 출처 데이터셋
- uspto-grants-2007_02
- 특허 번호
- US07176216B2
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