반응식
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([NH2:8])[N:3]=1.[I:9]N1C(=O)CCC1=O.O>CS(C)=O>[I:9][C:7]1[C:2]([NH2:1])=[N:3][C:4]([NH2:8])=[CH:5][CH:6]=1참가 물질
5
실험 절차
2,6-Diaminopyridine (100 g, 916 mmol) was dissolved in dimethyl sulfoxide (400 mL), and N-iodosuccinimide (100 g, 445 mmol) was added in one portion while stirring at room temperature. The reaction solution was stirring for 10 minutes at room temperature. Water (3.5 L) was added to the reaction solution, and the precipitated solids were filtered out. The resulting aqueous layer was extracted with ethyl acetate (1.3 L) 3 times. The ethyl acetate layers were combined and the solvent was evaporated under a reduced pressure. The residue was purified by silica gel chromatography (heptane:ethyl acetate=2:3) to obtain the title compound (23.8 g, 22.8%).
후처리
- stirringThe reaction solution was stirring for 10 minutes at room temperature
- filtrationthe precipitated solids were filtered out
- extractionThe resulting aqueous layer was extracted with ethyl acetate (1.3 L) 3 times
- customthe solvent was evaporated under a reduced pressure
- customThe residue was purified by silica gel chromatography (heptane:ethyl acetate=2:3)
출처 및 근거
- ORD 기록
- ord-3aa85e0c537f40388de71e7309cd7eb1
- 출처 데이터셋
- uspto-grants-2014_09
- 특허 번호
- US08841327B2
연결된 노트
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