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

HRID 2047597
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HRID 2047597 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]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

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
18 °C

실험 절차

To a solution of 5-bromo-2,3-dimethoxypyridine (4-2, 0.300 g, 1.38 mmol, 1.0 equiv) in dimethylformamide (3.9 mL) was added copper (I) cyanide (0.15 gL, 1.65 mmol, 1.2 equiv) and the reaction mixture was heated for 40 minutes at 18° 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 (4-3) 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-f3d56d35b8d94f3ca2295f5a827bf4c8
출처 데이터셋
uspto-grants-2013_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08592457B2

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