Ammonium formate → Methyl 3-amino-5-fluoro-4-methylbenzoate

HRID 1697343노트

반응식

HRID 1697343 반응식
[CH3:1][O:2][C:3](=[O:16])[C:4]1[CH:9]=[C:8]([F:10])[C:7]([CH3:11])=[C:6]([N+:12]([O-])=O)[C:5]=1Cl.C([O-])=O.[NH4+]>C(O)C.[Pd]>[CH3:1][O:2][C:3](=[O:16])[C:4]1[CH:9]=[C:8]([F:10])[C:7]([CH3:11])=[C:6]([NH2:12])[CH:5]=1

참가 물질

5

반응물 2

HCID 2723923Ammonium formateHCID 866615862-Chloro-5-fluoro-4-methyl-3-nitro-benzoic acid methyl ester

생성물 1

HCID 47002571Methyl 3-amino-5-fluoro-4-methylbenzoate수율 88.5%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

반응 조건

온도
75 °C

실험 절차

2-Chloro-5-fluoro-4-methyl-3-nitro-benzoic acid methyl ester (Example 252d, 53 g), 5% Pd/C (9 g) and ammonium formate (80 g) were stirred together in ethanol (500 mL) at 75° C. for 32 h. The reaction was filtered through celite and filtrate evaporated to a solid. This solid residue was dissolved in dichloromethane, washed with water. The separated aqueous layer was further extracted with dichloromethane (3×100 mL) and the combined organics dried (MgSO4) and evaporated. Analysis showed significant unreacted starting material. The reaction was repeated by new 5% P/C (9 g) and ammonium formate (80 g) together in ethanol (500 mL) and heating at 75° C. for 20 h. Further 5% Pd/C (9 g) and ammonium formate (80 g) were added and heating continued for 10 h. The mixture was filtered through celite and the filter cake was washed with further ethanol. The combined filtrates were evaporated, the residue dissolved in dichloromethane, washed with water. The separated aqueous layer was further extracted with dichloromethane (3×100 mL) and the combined organics dried (MgSO4) and evaporated to afford the subtitle compound (34.7 g).

후처리

  1. filtrationThe reaction was filtered through celite and filtrate
  2. customevaporated to a solid
  3. dissolutionThis solid residue was dissolved in dichloromethane
  4. washwashed with water
  5. extractionThe separated aqueous layer was further extracted with dichloromethane (3×100 mL)
  6. dry with materialthe combined organics dried (MgSO4)
  7. customevaporated
  8. additionFurther 5% Pd/C (9 g) and ammonium formate (80 g) were added
  9. temperatureheating
  10. filtrationThe mixture was filtered through celite
  11. washthe filter cake was washed with further ethanol
  12. customThe combined filtrates were evaporated
  13. dissolutionthe residue dissolved in dichloromethane
  14. washwashed with water
  15. extractionThe separated aqueous layer was further extracted with dichloromethane (3×100 mL)
  16. dry with materialthe combined organics dried (MgSO4)
  17. customevaporated

출처 및 근거

ORD 기록
ord-3b7794c632f34c629bf04017161896e3
출처 데이터셋
uspto-grants-2012_04
특허 번호
US08163905B2

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