Hydrogen Bromide → Ethyl 6-(5'-chloro-2'-hydroxy-2-biphenylyl)-2-pyridinecarboxylate
반응식
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([O:25]CC2C=CC=CC=2)=[C:6]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=2[C:14]2[N:19]=[C:18]([C:20]([O:22][CH2:23][CH3:24])=[O:21])[CH:17]=[CH:16][CH:15]=2)[CH:7]=1.Br>C(O)(=O)C.C(OCC)C.O.C(=O)([O-])[O-].[K+].[K+]>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([OH:25])=[C:6]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=2[C:14]2[N:19]=[C:18]([C:20]([O:22][CH2:23][CH3:24])=[O:21])[CH:17]=[CH:16][CH:15]=2)[CH:7]=1참가 물질
반응물 2
생성물 1
시약·촉매·용매 3
실험 절차
Ethyl 6-{5′-chloro-2′-[(phenylmethyl)oxy]-2-biphenylyl}-2-pyridinecarboxylate (1.22 g, 2.75 mmol) was dissolved in acetic acid (5 ml) and 48% hydrogen bromide in acetic acid (5 ml), left at room temperature for 0.5 hours then diluted with diethyl ether/water and basified with potassium carbonate. The organic phase was separated, dried (magnesium sulphate), evaporated and chromatographed on silica eluting with ethyl acetate/iso-hexane (1:3). The product was dissolved in ethanol (20 ml), 60% sodium hydride (2 mg) added and the solution left at room temperature for 16 hours. The resulting solution was acidified with acetic acid, diluted with water/ether and the organic phase washed with saturated sodium bicarbonate solution, dried (magnesium sulphate), evaporated and chromatographed on silica to give 801 mg of colourless gum. LC/MS t=3.33, [MH+] 354.3, 356.3
후처리
- customThe organic phase was separated
- dry with materialdried (magnesium sulphate)
- customevaporated
- customchromatographed on silica eluting with ethyl acetate/iso-hexane (1:3)
- dissolutionThe product was dissolved in ethanol (20 ml)
- addition60% sodium hydride (2 mg) added
- additiondiluted with water/ether
- washthe organic phase washed with saturated sodium bicarbonate solution
- dry with materialdried (magnesium sulphate)
- customevaporated
- customchromatographed on silica
출처 및 근거
- ORD 기록
- ord-1e4a5cd055694557863d99c843dba142
- 출처 데이터셋
- uspto-grants-2008_11
- 특허 번호
- US07446222B2
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