Hydrochloric Acid → HCID 59395032, 화합물

HRID 1931327노트

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HRID 1931327 반응식
[N+:1]([C:4]1[CH:9]=[C:8]([N+:10]([O-])=O)[CH:7]=[CH:6][C:5]=1[C:13]([OH:22])([C:18]([F:21])([F:20])[F:19])[C:14](OC)=[O:15])([O-])=O.Cl>C(OCC)(=O)C>[NH2:10][C:8]1[CH:9]=[C:4]2[C:5]([C:13]([OH:22])([C:18]([F:21])([F:20])[F:19])[C:14](=[O:15])[NH:1]2)=[CH:6][CH:7]=1

참가 물질

4

실험 절차

To a solution of methyl 2-(2,4-dinitrophenyl)-3,3,3-trifluoro-2-hydroxypropanoate (1.3 g, 4.01 mmol) in ethyl acetate (18 mL) was successively added pH3 HCl (5.2 mL), then PdC (350 mg) in ethyl acetate (3 mL). The mixture was vigorously stirred overnight under H2 (1 atm). The catalyst was filtered off through Celite and the filtrate was concentrated to dryness. The crude residue obtained was partitioned between DCM (25 mL) and aqueous saturated NaHCO3 (15 mL). The organic phase was separated and the aqueous phase was extracted DCM (2×25 mL). The organic phases were combined, dried over sodium sulfate, filtered, and concentrated. The crude residue obtained was purified by silica gel column chromatography using a gradient 50-100% ethyl acetate in hexanes to give 6-amino-3-hydroxy-3-(trifluoromethyl)indolin-2-one (921 mg, 99%)

후처리

  1. filtrationThe catalyst was filtered off through Celite
  2. concentrationthe filtrate was concentrated to dryness
  3. customThe crude residue obtained
  4. customwas partitioned between DCM (25 mL) and aqueous saturated NaHCO3 (15 mL)
  5. customThe organic phase was separated
  6. extractionthe aqueous phase was extracted DCM (2×25 mL)
  7. dry with materialdried over sodium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated
  10. customThe crude residue obtained
  11. customwas purified by silica gel column chromatography

출처 및 근거

ORD 기록
ord-262892e3e6294c32b8826dcdb5f42e33
출처 데이터셋
uspto-grants-2012_05
특허 번호
US08188283B2

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