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Methyl iodide → 6-Amino-4-methoxy-2-methylnicotinonitrile

HRID 928387
ノート
印刷プレビュー

反応式

HRID 928387 の反応式
[NH2:1][C:2]1[N:7]=[C:6]([CH3:8])[C:5]([C:9]#[N:10])=[C:4]([O-:11])[CH:3]=1.[Na+].[C:13]([O-])([O-])=O.[K+].[K+].CI.C([O-])(O)=O.[Na+]>CN(C=O)C>[NH2:1][C:2]1[CH:3]=[C:4]([O:11][CH3:13])[C:5]([C:9]#[N:10])=[C:6]([CH3:8])[N:7]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 6328Methyl iodideHCID 11430Potassium CarbonateHCID 516892Sodium BicarbonateHCID 58081220Sodium 6-amino-3-cyano-2-methylpyridin-4-olate

生成物 1

HCID 667237286-Amino-4-methoxy-2-methylnicotinonitrile

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

To a mixture of sodium 6-amino-3-cyano-2-methylpyridin-4-olate (500 mg, 2.92 mmol, prepared in analogy to WO2001062233A2 and isolated as sodium salt), and K2CO3 (808 mg, 5.84 mmol) in DMF (1 ml) was added MeI (0.200 ml, 3.21 mmol), and the reaction mixture was stirred at it for 9 d. Saturated NaHCO3 (50 ml) was added and the mixture was extracted with EA (4×20 ml). The combined organic extracts were diluted with additional DCM and MeOH until homogeneous, dried over Na2SO4, filtered and concentrated. The crude product was recrystallized from refluxing MeOH-DCM to afford the title compound. 1H-NMR (DMSO-d6, 400 MHz): 2.34 (s, 3H), 3.82 (s, 3H), 5.91 (s, 1H), 6.83 (br, s, 2H); LCMS RtM=1.11 min, [M+H]+=164.2.

後処理

  1. extractionthe mixture was extracted with EA (4×20 ml)
  2. additionThe combined organic extracts were diluted with additional DCM and MeOH until homogeneous,
  3. dry with materialdried over Na2SO4
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customThe crude product was recrystallized
  7. temperaturefrom refluxing MeOH-DCM

出典と根拠

ORDレコード
ord-a063049e807e44a6947682d2b269d4ee
出典データセット
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09290485B2

反応ノート

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