2-(2-bromophenyl)-3-methyl-2H-azirine → 4-Bromo-2-methyl-1H-indole
반응식
[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH:8]1[C:10]([CH3:11])=[N:9]1>C1(C)C(C)=CC=CC=1>[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]2[C:3]=1[CH:8]=[C:10]([CH3:11])[NH:9]2참가 물질
3
실험 절차
The solution of 2-(2-bromophenyl)-3-methyl-2H-azirine (758 mg, 3.61 mmol) in xylene (20 mL) was stirred at 160° C. for 7 d. The reaction mixture was concentrated in vacuo. The residue was purified by SiO2 chromatography eluting with petroleum ether/EtOAc (10:1) to afford 4-bromo-2-methyl-1H-indole as yellow oil (572 mg, 75.5%). MS (ESI): m/z=210.1 [M+1]+.
후처리
- concentrationThe reaction mixture was concentrated in vacuo
- customThe residue was purified by SiO2 chromatography
- washeluting with petroleum ether/EtOAc (10:1)
출처 및 근거
- ORD 기록
- ord-a2cea392b0b44911ae2ad43a2a5142e0
- 출처 데이터셋
- uspto-grants-2014_01
- 특허 번호
- US08637537B2
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