Water → HCID 89444094, 화합물

HRID 1771737노트

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HRID 1771737 반응식
[F:1][C:2]1[CH:10]=[CH:9][C:8]([C:11]2[CH:16]=[CH:15][CH:14]=[C:13]([F:17])[CH:12]=2)=[CH:7][C:3]=1[C:4]([OH:6])=O.O=S(Cl)Cl.[NH2:22][C:23]1[C:24]([F:32])=[C:25]([OH:31])[CH:26]=[C:27]([CH3:30])[C:28]=1[F:29].O>C(Cl)Cl.CN(C=O)C.C1COCC1>[F:32][C:24]1[C:25]([OH:31])=[CH:26][C:27]([CH3:30])=[C:28]([F:29])[C:23]=1[NH:22][C:4](=[O:6])[C:3]1[CH:7]=[C:8]([C:11]2[CH:16]=[CH:15][CH:14]=[C:13]([F:17])[CH:12]=2)[CH:9]=[CH:10][C:2]=1[F:1]

참가 물질

8

실험 절차

To a solution of 2-fluoro-5-(3-fluorophenyl)benzoic acid (Intermediate III(a)) (437 mg, 1.87 mmol, 1.1 eq) in CH2Cl2 (10 mL) and DMF (3 drops) was added SOCl2 (15 mL) dropwise at 0° C. The solution was stirred at room temperature for 1 h, then concentrated in vacuo. The residue obtained was dissolved in THF (20 mL) and added dropwise to a solution of 3-amino-2,4-difluoro-5-methyl-phenol (270 mg, 1.70 mmol, 1.0 eq) in THF (10 mL) at 0° C. After addition was completed, the reaction mixture was stirred at room temperature for 2 h, then poured into water and extracted with EtOAc. The combined organic extracts were washed with water and brine, dried (Na2SO4), filtered, and evaporated in vacuo. The residue obtained was purified by column chromatography (petroleum ether: EtOAc, 10:1 to 3:1) to give the title compound as a white solid (285 mg, 45%).

후처리

  1. concentrationconcentrated in vacuo
  2. customThe residue obtained
  3. additionAfter addition
  4. stirringthe reaction mixture was stirred at room temperature for 2 h
  5. extractionextracted with EtOAc
  6. washThe combined organic extracts were washed with water and brine
  7. dry with materialdried (Na2SO4)
  8. filtrationfiltered
  9. customevaporated in vacuo
  10. customThe residue obtained
  11. customwas purified by column chromatography (petroleum ether: EtOAc, 10:1 to 3:1)

출처 및 근거

ORD 기록
ord-552f183a47ca4dfa8a57912769315f05
출처 데이터셋
uspto-grants-2016_02
특허 번호
US09249085B2

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