Methyl triflate → HCID 178448620、化合物

HRID 1931100

反応式

HRID 1931100 の反応式
[CH2:1]([N:5]1[C:9]([NH:10][C:11](=[O:23])[C:12]2[CH:17]=[C:16]([C:18]([F:21])([F:20])[F:19])[CH:15]=[CH:14][C:13]=2[F:22])=[CH:8][C:7]([C:24]([CH3:27])([CH3:26])[CH3:25])=[N:6]1)[CH2:2][CH2:3][CH3:4].F[C:29](F)(F)S(OC)(=O)=O.[NH4+].[OH-]>C1(C)C=CC=CC=1.O.CC(C)=O>[CH2:1]([N:5]1[N:6]([CH3:29])[C:7]([C:24]([CH3:26])([CH3:25])[CH3:27])=[CH:8]/[C:9]/1=[N:10]\[C:11](=[O:23])[C:12]1[CH:17]=[C:16]([C:18]([F:19])([F:21])[F:20])[CH:15]=[CH:14][C:13]=1[F:22])[CH2:2][CH2:3][CH3:4]

参加物

7

反応物 3

HCID 9526Methyl triflateHCID 14923Ammonium HydroxideHCID 66643255n-(1-Butyl-3-tert-butyl-1h-pyrazol-5-yl)-2-fluoro-5-(trifluoromethyl)benzamide

生成物 1

HCID 178448620HCID 178448620、化合物収率 89.2%

試薬・触媒・溶媒 3

HCID 180Acetone溶媒HCID 962Water溶媒HCID 1140Toluene溶媒

反応条件

温度
100 °C

実験手順

To a solution of Example 81B (50.2 g, 130 mmol) in toluene (500 mL) was added methyl trifluoromethanesulfonate (21.4 mL, 195 mmol). The mixture was warmed to 100° C. and stirred for 20 hours. The mixture was cooled to ambient temperature then diluted with water (200 mL) and acetone (500 mL). This solution was stirred for 30 minutes then concentrated NH4OH (100 mL) was added. The mixture was stirred for 30 minutes then partially concentrated under reduced pressure. The residue was diluted with EtOAc (300 mL) and brine (100 mL), the layers were separated and the aqueous phase was extracted with EtOAc (3×30 mL). The combined organic extracts were dried over anhydrous Na2SO4, filtered, and concentrated under reduced pressure. The residue was purified by column chromatography (SiO2, 80% hexanes/EtOAc to 100% EtOAc to 10% MeOH in EtOAc) and the fractions collected and concentrated. The material was then dissolved in EtOAc (150 mL) and was washed with 10% NaOH (100 mL). The layers were separated, the aqueous phase was extracted with EtOAc (3×50 mL) and the combined organic extracts were dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure to give (46.3 g, 116 mmol, 89% yield) the title compound. MS (ESI+) m/z 400 (M+H)+.

後処理

  1. temperatureThe mixture was cooled to ambient temperature
  2. stirringThis solution was stirred for 30 minutes
  3. stirringThe mixture was stirred for 30 minutes
  4. concentrationthen partially concentrated under reduced pressure
  5. additionThe residue was diluted with EtOAc (300 mL) and brine (100 mL)
  6. customthe layers were separated
  7. extractionthe aqueous phase was extracted with EtOAc (3×30 mL)
  8. dry with materialThe combined organic extracts were dried over anhydrous Na2SO4
  9. filtrationfiltered
  10. concentrationconcentrated under reduced pressure
  11. customThe residue was purified by column chromatography (SiO2, 80% hexanes/EtOAc to 100% EtOAc to 10% MeOH in EtOAc)
  12. customthe fractions collected
  13. concentrationconcentrated
  14. dissolutionThe material was then dissolved in EtOAc (150 mL)
  15. washwas washed with 10% NaOH (100 mL)
  16. customThe layers were separated
  17. extractionthe aqueous phase was extracted with EtOAc (3×50 mL)
  18. dry with materialthe combined organic extracts were dried over anhydrous Na2SO4
  19. filtrationfiltered
  20. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-2cddeff4f71640339059b301b7c92dd1
出典データセット
uspto-grants-2012_05
特許番号
US08188135B2

関連ノート

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