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Ethyl Acetate → HCID 178428363, 화합물

HRID 1920880
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HRID 1920880 반응식
[F:1][C:2]([F:14])([F:13])[C:3]([C:5]1[C:6](F)=[N:7][CH:8]=[CH:9][C:10]=1I)=O.O.[NH2:16][NH2:17].[CH3:18]COC(C)=O.C([O-])(O)=O.[Na+].[Cl-].[Na+].O>O1CCOCC1>[CH3:18][C:10]1[CH:9]=[CH:8][N:7]=[C:6]2[NH:16][N:17]=[C:3]([C:2]([F:14])([F:13])[F:1])[C:5]=12
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 8857Ethyl AcetateHCID 24654Hydrazine hydrate (1:1)HCID 579695632,2,2-Trifluoro-1-(2-fluoro-4-iodopyridin-3-yl)ethanoneHCID 129703874Sodium hydrogencarbonate brine

생성물 1

HCID 178428363HCID 178428363, 화합물수율 73%

시약·촉매·용매 1

HCID 31275
1,4-Dioxane
용매

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온도
90 °C

실험 절차

2,2,2-trifluoro-1-(2-fluoro-4-iodo-3-pyridyl)ethanone (40 g, 125.4 mmol) was dissolved in 1,4-dioxane (300 mL). Hydrazine monohydrate (18.83 g, 18.30 mL, 376.2 mmol) was added dropwise and the mixture heated to 90° C. for 90 minutes. The mixture was cooled and poured into EtOAc (800 ml) and 3:1 sat NaHCO3/brine (500 ml). The organic layer was separated and the aqueous extracted with EtOAc (3×50 ml). The combined organics were washed with brine (100 ml), dried (MgSO4), filtered and concentrated. The residue was slurried in DCM (50 ml) and the resultant white solid was isolated by filtration, washed with DCM and dried (28.7 g, 73% Yield).

후처리

  1. temperatureThe mixture was cooled
  2. customThe organic layer was separated
  3. extractionthe aqueous extracted with EtOAc (3×50 ml)
  4. washThe combined organics were washed with brine (100 ml)
  5. dry with materialdried (MgSO4)
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customthe resultant white solid was isolated by filtration
  9. washwashed with DCM
  10. customdried (28.7 g, 73% Yield)

출처 및 근거

ORD 기록
ord-82b4d046c9144d6587cb6ba1ca268e84
출처 데이터셋
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08173635B2

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