Dimethylformamide dimethyl acetal → HCID 178423428、化合物

HRID 241683

反応式

HRID 241683 の反応式
[Cl:1][C:2]1[CH:3]=[C:4]([CH:8]=[C:9]([CH3:11])[N:10]=1)[C:5]([NH2:7])=O.COC(OC)[N:15]([CH3:17])C.C(O)(=O)C.[NH2:24]N>CN(C=O)C.C(O)(=O)C>[Cl:1][C:2]1[CH:3]=[C:4]([C:5]2[N:15]=[CH:17][NH:24][N:7]=2)[CH:8]=[C:9]([CH3:11])[N:10]=1

参加物

6

反応条件

温度
90 °C

実験手順

2-Chloro-6-methyl-isonicotinamide (1.23 g) and N,N-dimethylformamide dimethyl acetal (1.05 ml) were dissolved in dry DMF (4 ml) under inert atmosphere and the resulting solution was heated to 90° C. and stirred for 1 h. The reaction mixture was cooled to room temperature and a solution of hydrazine acetate (3.32 g) in acetic acid (8 ml) was dropwise added. The mixture was heated to 90° C. and stirred for 1 h. The solvent was removed under reduced pressure and the residue partitioned between saturated aqueous solution of NaHCO3 and EtOAc. The organic phase was separated, washed with brine, dried under Na2SO4, filtered and the solvent was evaporated under reduced pressure. The crude was purified by flash column chromatography (10 g Isolute® silica gel cartridge; gradient elution: hexane/EtOAc from 1/1 to 3/7) affording 2-Chloro-6-methyl-4-(1H-[1,2,4]triazol-3-yl)-pyridine (0.92 g). GC (Rt)=13.21 min (method=3A)

後処理

  1. temperatureThe reaction mixture was cooled to room temperature
  2. temperatureThe mixture was heated to 90° C.
  3. stirringstirred for 1 h
  4. customThe solvent was removed under reduced pressure
  5. customthe residue partitioned between saturated aqueous solution of NaHCO3 and EtOAc
  6. customThe organic phase was separated
  7. washwashed with brine
  8. customdried under Na2SO4
  9. filtrationfiltered
  10. customthe solvent was evaporated under reduced pressure
  11. customThe crude was purified by flash column chromatography (10 g Isolute® silica gel cartridge; gradient elution: hexane/EtOAc from 1/1 to 3/7)

出典と根拠

ORDレコード
ord-2dca4ae63771481594945def71eabcb5
出典データセット
uspto-grants-2014_02
特許番号
US08653075B2

関連ノート

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