Pyridine → HCID 58374105, 화합물

HRID 1506307노트

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HRID 1506307 반응식
[C:1]1([C:7]2[O:11][N:10]=[C:9]([C:12](O)=[O:13])[C:8]=2[C:15]([F:18])([F:17])[F:16])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.N1C=CC=CC=1.N1C(F)=NC(F)=NC=1[F:27]>ClCCl>[C:1]1([C:7]2[O:11][N:10]=[C:9]([C:12]([F:27])=[O:13])[C:8]=2[C:15]([F:18])([F:17])[F:16])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

참가 물질

5

실험 절차

To a mixture of 5-phenyl-4-(trifluoromethyl)isoxazole-3-carboxylic acid (I-5D, 197 mg, 0.766 mmol) and pyridine (0.074 mL, 0.919 mmol) in dichloromethane (5 mL) at room temperature was added cyanuric fluoride (0.078 mL, 0.919 mmol). The reaction mixture was stirred at room temperature for 18 h. The mixture was diluted with dichloromethane (40 mL) and washed with an ice-cold 0.5N aqueous solution of hydrochloric acid (20 mL). The aqueous layer was extracted with dichloromethane (20 mL), and the combined organic layers were washed with ice-cold water (20 mL) and dried over anhydrous magnesium sulfate. Concentration under reduced pressure afforded 5-phenyl-4-(trifluoromethyl)isoxazole-3-carbonyl fluoride (199 mg, 0.768 mmol, 100% yield) as a pale yellow oil. The compound had an HPLC retention time=2.53 min. (methyl ester)-Column: Chromolith SpeedROD 4.6×50 mm (4 min.); Solvent A=10% MeOH, 90% H2O, 0.1% TFA; Solvent B=90% MeOH, 10% H2O, 0.1% TFA.

후처리

  1. washwashed with an ice-cold 0.5N aqueous solution of hydrochloric acid (20 mL)
  2. extractionThe aqueous layer was extracted with dichloromethane (20 mL)
  3. washthe combined organic layers were washed with ice-cold water (20 mL)
  4. dry with materialdried over anhydrous magnesium sulfate
  5. concentrationConcentration under reduced pressure

출처 및 근거

ORD 기록
ord-33eefe29c53c46e088b680058c574da7
출처 데이터셋
uspto-grants-2015_12
특허 번호
US09216972B2

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