Dimethyl Disulfide → 5-(methylthio)-1-(4-vinylphenyl)-1H-1,2,4-triazole
반응식
[CH:1]([C:3]1[CH:8]=[CH:7][C:6]([N:9]2[CH:13]=[N:12][CH:11]=[N:10]2)=[CH:5][CH:4]=1)=[CH2:2].[Li]CCCC.[CH3:19][S:20]SC>C1COCC1>[CH3:19][S:20][C:13]1[N:9]([C:6]2[CH:5]=[CH:4][C:3]([CH:1]=[CH2:2])=[CH:8][CH:7]=2)[N:10]=[CH:11][N:12]=1참가 물질
실험 절차
To a stirred solution of 1-(4-vinyl-phenyl)-1H-[1,2,4]-triazole (1 g, 5.8 mmol) in 50 mL of THF, was added n-BuLi (0.41 g, 6.4 mmol) at −78° C. and stirred for 30 min. To this dimethyldisulfide in THF (0.6 g, 6.43 mmol) was added and the resultant reaction mixture was stirred at ambient temperature for 16 h. The reaction mixture was quenched with a saturated aqueous NH4Cl solution and extracted with EtOAc (3×25 mL). The combined EtOAc layer was washed with brine and dried over sodium sulphate and concentrated under reduced pressure. The crude compound was purified by flash chromatography (SiO2, 100-200 mesh, 40% EtOAc in Pet ether) to afford the title compound as an off white solid (0.6 g, 48%): mp 68-70° C.; 1H NMR (400 MHz, CDCl3) δ 7.96 (s, 1H), 7.05 (m, 4H), 6.75 (dd, J=16.4, 10.7 Hz, 1H), 5.81 (d, J=16.4 Hz, 1H), 5.35 (d, J=10.7 Hz, 1H), 2.73 (s, 3H); ESIMS m/z 218.09 ([M+H]+).
후처리
- customthe resultant reaction mixture
- stirringwas stirred at ambient temperature for 16 h
- customThe reaction mixture was quenched with a saturated aqueous NH4Cl solution
- extractionextracted with EtOAc (3×25 mL)
- washThe combined EtOAc layer was washed with brine
- dry with materialdried over sodium sulphate
- concentrationconcentrated under reduced pressure
- customThe crude compound was purified by flash chromatography (SiO2, 100-200 mesh, 40% EtOAc in Pet ether)
출처 및 근거
- ORD 기록
- ord-1145e33230ba492d87b85e1d17376e34
- 출처 데이터셋
- uspto-grants-2015_12
- 특허 번호
- US09215870B2
반응 노트
불러오는 중…