HCID 86694125、化合物 → 2-Chloro-5-fluoro-N-methylpyridin-3-amine

HRID 707244ノート

反応式

HRID 707244 の反応式
[Cl:1][C:2]1[C:7]([N:8](C)[C:9](=O)OC(C)(C)C)=[CH:6][C:5]([F:17])=[CH:4][N:3]=1>FC(F)(F)C(O)=O>[Cl:1][C:2]1[C:7]([NH:8][CH3:9])=[CH:6][C:5]([F:17])=[CH:4][N:3]=1

参加物

3

反応条件

温度
50 °C

実験手順

Tert-butyl (2-chloro-5-fluoropyridin-3-yl)(methyl)carbamate (Intermediate 36) (0.920 g, 3.53 mmol) was dissolved in trifluoroacetic acid (20 mL) and heated at 50° C. for 90 minutes. The solution was allowed to cool to room temperature and stir for another 14 hours. The reaction mixture was evaporated to dryness under reduced pressure and water (80 mL), saturated sodium bicarbonate (50 mL) and ethyl acetate (100 mL) were added. The phases were mixed and separated and the organic phase was dried with magnesium sulfate before evaporating to dryness under reduced pressure. Purification using silica chromatography (0-10% methanol in dichloromethane gradient) gave 2-chloro-5-fluoro-N-methylpyridin-3-amine as an oil.

後処理

  1. temperatureto cool to room temperature
  2. customThe reaction mixture was evaporated to dryness under reduced pressure and water (80 mL), saturated sodium bicarbonate (50 mL) and ethyl acetate (100 mL)
  3. additionwere added
  4. additionThe phases were mixed
  5. customseparated
  6. dry with materialthe organic phase was dried with magnesium sulfate
  7. custombefore evaporating to dryness under reduced pressure
  8. customPurification

出典と根拠

ORDレコード
ord-c028ee69fe4d420698c4a8027cf0c324
出典データセット
uspto-grants-2015_11
特許番号
US09174992B2

反応ノート

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