Dimethylformamide → Methyl 2-chloro-6-methylpyridine-3-carboxylate

HRID 347628

反応式

HRID 347628 の反応式
[Cl:1][C:2]1[N:10]=[C:9]([CH3:11])[CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].[CH3:12]N(C=O)C.C(Cl)(=O)C(Cl)=O>ClCCl>[Cl:1][C:2]1[N:10]=[C:9]([CH3:11])[CH:8]=[CH:7][C:3]=1[C:4]([O:6][CH3:12])=[O:5]

参加物

5

実験手順

To a suspension of 2-chloro-6-methylnicotinic acid (5.3 g, 30.8 mmol) in dichloromethane (100 ml) at 0° C. were added DMF (1 ml) and oxalyl chloride (3.2 ml, 36.9 mmol). The mixture was allowed to warmn to room temperature and stirred for 5 h. The solvents were removed in vacuo and the residue was dissolved in dichloromethane (50 ml) and methanol (50 ml). The mixture was stirred at room temperature for 18 h and then concentrated in vacuo. The residue was dissolved in chloroform, washed with saturated sodium bicarbonate solution and brine, dried over MgSO4, and concentrated in vacuo to give a brown oil; yield 5.70 g (100%).

後処理

  1. customto warmn to room temperature
  2. customThe solvents were removed in vacuo
  3. dissolutionthe residue was dissolved in dichloromethane (50 ml)
  4. stirringThe mixture was stirred at room temperature for 18 h
  5. concentrationconcentrated in vacuo
  6. dissolutionThe residue was dissolved in chloroform
  7. washwashed with saturated sodium bicarbonate solution and brine
  8. dry with materialdried over MgSO4
  9. concentrationconcentrated in vacuo
  10. customto give a brown oil

出典と根拠

ORDレコード
ord-e8a38c9878e446839eb2daf1c59b6e4a
出典データセット
uspto-grants-2007_02
特許番号
US07176195B2

関連ノート

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