Trifluoroacetic acid → 3,5-Dimethylpyridin-2-amine

HRID 594100

反応式

HRID 594100 の反応式
[CH3:1][C:2]1[C:3]([NH:9]C(C)(CC(C)(C)C)C)=[N:4][CH:5]=[C:6]([CH3:8])[CH:7]=1.FC(F)(F)C(O)=O>>[CH3:1][C:2]1[C:3]([NH2:9])=[N:4][CH:5]=[C:6]([CH3:8])[CH:7]=1

参加物

3

反応条件

温度
50 °C

実験手順

3,5-dimethyl-N-(2,4,4-trimethylpentan-2-yl)pyridin-2-amine (6.5 g, 27.7 mmol) was mixed with 2,2,2-trifluoroacetic acid (46 mL, 621 mmol) and heated to 50° C. for 4.5 hours. The mixture was concentrated in vacuo then diluted with dichloromethane (10 mL) and water (10 mL). The layers were partioned and aqueous phase was neutralised to pH 7-8 using saturated bicarbonate solution. The product was then extracted with dichloromethane (3×10 mL) and the organics were dried using a phase separator cartridge. The solvent was evaporated in vacuo to give the title compound (2.99 g) as a white solid. LCMS (2 min, High pH) Rt 0.69 min, m/z (ES+) 123 (M+H).

後処理

  1. concentrationThe mixture was concentrated in vacuo
  2. additionthen diluted with dichloromethane (10 mL) and water (10 mL)
  3. extractionThe product was then extracted with dichloromethane (3×10 mL)
  4. customthe organics were dried
  5. customThe solvent was evaporated in vacuo

出典と根拠

ORDレコード
ord-12402a79e13f45a6ba7c3ba17809153d
出典データセット
uspto-grants-2016_01
特許番号
US09242972B2

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