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5-Bromo-2,3-dimethoxypyridine → 5,6-Dimethoxypyridine-3-carbonitrile

HRID 1802334
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HRID 1802334 반응식
Br[C:2]1[CH:3]=[C:4]([O:10][CH3:11])[C:5]([O:8][CH3:9])=[N:6][CH:7]=1.[Cu][C:13]#[N:14]>CN(C)C=O>[CH3:11][O:10][C:4]1[C:5]([O:8][CH3:9])=[N:6][CH:7]=[C:2]([CH:3]=1)[C:13]#[N:14]
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참가 물질

4

반응물 2

HCID 125630845-Bromo-2,3-dimethoxypyridineHCID 178418546HCID 178418546, 화합물

생성물 1

HCID 467367595,6-Dimethoxypyridine-3-carbonitrile

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

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온도
180 °C

실험 절차

To a solution of 5-bromo-2,3-dimethoxypyridine (1-2, 0.300 g, 1.38 mmol, 1.0 equiv) in dimethylformamide (3.9 mL) was added copper (I) cyanide (0.15 g, 1.65 mmol, 1.2 equiv) and the reaction mixture was heated for 40 minutes at 180° C. in a microwave reactor. The reaction mixture was cooled and partitioned between EtOAc (50 mL) and water (50 mL). The organic phase was washed with water (2×30 mL) and brine (1×30 mL), dried over magnesium sulfate and concentrated. The residue was purified via normal phase chromatography (0 to 40% EtOAc in hexanes, silica) to afford the desired product (1-3) as white solid after concentration. ESI+MS [M+H]+ C8H8N2O2 calc'd 165.1. found 165.1.

후처리

  1. temperatureThe reaction mixture was cooled
  2. custompartitioned between EtOAc (50 mL) and water (50 mL)
  3. washThe organic phase was washed with water (2×30 mL) and brine (1×30 mL)
  4. dry with materialdried over magnesium sulfate
  5. concentrationconcentrated
  6. customThe residue was purified via normal phase chromatography (0 to 40% EtOAc in hexanes, silica)

출처 및 근거

ORD 기록
ord-cce85ead153c446e8d559946a5313203
출처 데이터셋
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08349872B2

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