Tetrahydrofuran → 4-(4-Acetamidophenyl)pyridine
반응식
C([O-])([O-])=O.[Na+].[Na+].C1COCC1.Cl.Br[C:14]1[CH:19]=[CH:18][N:17]=[CH:16][CH:15]=1.CC1(C)C(C)(C)OB([C:28]2[CH:33]=[CH:32][C:31]([NH:34][C:35](=[O:37])[CH3:36])=[CH:30][CH:29]=2)O1>CCOC(C)=O.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.Cl[Pd]Cl.[Fe+2]>[N:17]1[CH:18]=[CH:19][C:14]([C:28]2[CH:33]=[CH:32][C:31]([NH:34][C:35](=[O:37])[CH3:36])=[CH:30][CH:29]=2)=[CH:15][CH:16]=1참가 물질
7
반응물 4
생성물 1
시약·촉매·용매 2
실험 절차
A round bottom flask was charged with a 2 N Na2CO3 solution (4 equivalents) and THF and the mixture was sparged with N2 through a dispersion tube. 4-Bromopyridine hydrochloride (1 equivalent) and N-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]acetamide (1.2 equivalents) were subsequently added, followed by Pd(dppf)2Cl2 (2.5 mol %). The reaction mixture was refluxed overnight, cooled to room temperature and diluted with EtOAc. The two phases were separated and the organic phase was washed with a 2 N Na2CO3 solution, brine, and dried (Na2SO4). Evaporation of the solvent under reduced pressure and purification by silica gel chromatography afforded the desired product as a white solid. MH+=213.1.
후처리
- customthe mixture was sparged with N2 through a dispersion tube
- temperatureThe reaction mixture was refluxed overnight
- customThe two phases were separated
- washthe organic phase was washed with a 2 N Na2CO3 solution, brine
- dry with materialdried (Na2SO4)
- customEvaporation of the solvent
- customunder reduced pressure and purification by silica gel chromatography
출처 및 근거
- ORD 기록
- ord-545f5e64cb4f4346a7341e2ddcb4df07
- 출처 데이터셋
- uspto-grants-2010_11
- 특허 번호
- US07825132B2
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