1,2-Dimethoxyethane → 6-(3-Chloro-phenyl)-pyridine-2-carboxylic acid methyl ester

HRID 33536

반응식

HRID 33536 반응식
[Cl:1][C:2]1[CH:3]=[C:4](B2OC(C)(C)C(C)(C)O2)[CH:5]=[CH:6][CH:7]=1.[C:17](=[O:20])([O-])[O-:18].[Cs+].[Cs+].COC([C:27]1[CH:28]=[N:29][CH:30]=[C:31](Br)[CH:32]=1)=O.[CH2:34](COC)OC>C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1>[CH3:34][O:18][C:17]([C:28]1[CH:27]=[CH:32][CH:31]=[C:30]([C:4]2[CH:5]=[CH:6][CH:7]=[C:2]([Cl:1])[CH:3]=2)[N:29]=1)=[O:20]

참가 물질

6

실험 절차

104 mg (0.09 mmol)Pd(PPh3)4, 1.5 g (6.29 mmol) of 3-chlorophenylboronic acid pinacol ester 2.86 ml (8.58 mmol) and 3M cesium carbonate solution were added under argon at room temperature to a solution of 1.24 g (5.72 mmol) methyl-5-bromo-pyridine-3-carboxylate in 45 ml dimethoxyethane and the mixture was heated to reflux for 30 min. The reaction mixture was cooled to room temperature and evaporated. The residue was taken up with ethyl acetate, washed with water, dried over sodium sulphate and evaporated. Chromatography on silica (eluent: ethyl acetate/n-heptane 1:3) gave 1.42 g (83%) of 6-(3-Chloro-phenyl)-pyridine-2-carboxylic acid methyl ester

후처리

  1. temperaturethe mixture was heated
  2. temperatureto reflux for 30 min
  3. customevaporated
  4. washwashed with water
  5. dry with materialdried over sodium sulphate
  6. customevaporated

출처 및 근거

ORD 기록
ord-0a866843f27743d892c6a85afdab0db5
출처 데이터셋
uspto-grants-2008_09
특허 번호
US07429605B2

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