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N-bromobutanimide → 3-bromo-4-fluoro-5-(1-methyl-1H-pyrazol-4-yl)pyridin-2-amine

HRID 595851
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HRID 595851 반응식
[F:1][C:2]1[C:7]([C:8]2[CH:9]=[N:10][N:11]([CH3:13])[CH:12]=2)=[CH:6][N:5]=[C:4]([NH2:14])[CH:3]=1.C1C(=O)N([Br:22])C(=O)C1>C(#N)C>[Br:22][C:3]1[C:4]([NH2:14])=[N:5][CH:6]=[C:7]([C:8]2[CH:9]=[N:10][N:11]([CH3:13])[CH:12]=2)[C:2]=1[F:1]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 67184N-bromobutanimideHCID 1180463264-fluoro-5-(1-methyl-1H-pyrazol-4-yl)pyridin-2-amine

생성물 1

HCID 1180452043-bromo-4-fluoro-5-(1-methyl-1H-pyrazol-4-yl)pyridin-2-amine수율 14.2%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

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온도
0 °C

실험 절차

To a solution of 4-fluoro-5-(1-methyl-1H-pyrazol-4-yl)pyridin-2-amine (150 mg, 0.780 mmol) in acetonitrile (7. 805 mL) was added NBS (142 mg, 0.796 mmol) in three portions at 0° C. The reaction mixture was stirred at 0° C. for 20 min. LCMS showed the reaction complete. After quenched with sat Na2SO3 and NaHCO3, stirred for 30 min. The reaction mixture was extracted with EtOAc 3 times. Filtered out solid. The solid was not the desired product. The EtOAc layers were washed by sat NaHCO3, water and brine. Dried and concentrated. The crude material was purified with flash chromatography eluting with 0-100% EtOAc (containing 10% MeOH/heptane to provide 30 mg of desired product. LCMS (m/z): 273.1 (MH+), 0.46 min.

후처리

  1. customthe reaction complete
  2. customAfter quenched with sat Na2SO3 and NaHCO3
  3. stirringstirred for 30 min
  4. extractionThe reaction mixture was extracted with EtOAc 3 times
  5. filtrationFiltered out solid
  6. washThe EtOAc layers were washed
  7. customDried
  8. concentrationconcentrated
  9. customThe crude material was purified with flash chromatography
  10. washeluting with 0-100% EtOAc (
  11. additioncontaining 10% MeOH/heptane

출처 및 근거

ORD 기록
ord-3b4eb4f2fd06407bb6a0fd71c7d1b625
출처 데이터셋
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09242996B2

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