Pyridine → HCID 58374105、化合物

HRID 1506307ノート

反応式

HRID 1506307 の反応式
[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

参加物

5

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-33eefe29c53c46e088b680058c574da7
出典データセット
uspto-grants-2015_12
特許番号
US09216972B2

反応ノート

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