HCID 86694125, 화합물 → 2-Chloro-5-fluoro-N-methylpyridin-3-amine

HRID 707244노트

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HRID 707244 반응식
[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

참가 물질

3

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온도
50 °C

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-c028ee69fe4d420698c4a8027cf0c324
출처 데이터셋
uspto-grants-2015_11
특허 번호
US09174992B2

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