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Ethyl Acetate → HCID 178428363、化合物

HRID 1920880
ノート
印刷プレビュー

反応式

HRID 1920880 の反応式
[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
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

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

生成物 1

HCID 178428363HCID 178428363、化合物収率 73%

試薬・触媒・溶媒 1

HCID 31275
1,4-Dioxane
溶媒

反応条件

温度
90 °C

実験手順

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).

後処理

  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)

出典と根拠

ORDレコード
ord-82b4d046c9144d6587cb6ba1ca268e84
出典データセット
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08173635B2

反応ノート

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