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

HRID 1802334
ノート
印刷プレビュー

反応式

HRID 1802334 の反応式
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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 125630845-Bromo-2,3-dimethoxypyridineHCID 178418546HCID 178418546、化合物

生成物 1

HCID 467367595,6-Dimethoxypyridine-3-carbonitrile

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
180 °C

実験手順

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.

後処理

  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)

出典と根拠

ORDレコード
ord-cce85ead153c446e8d559946a5313203
出典データセット
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08349872B2

反応ノート

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