تفاعل #657311

ord-5fdc646e557142ff9c0d88ee8192ca33

معادلة التفاعل

Oc1cc(-c2ccc(F)cc2)n[nH]1
3-(4-fluorophenyl)-1H-pyrazol-5-ol
O=C([O-])[O-].[K+].[K+]
K2CO3
CC(OS(C)(=O)=O)C(C)OS(C)(=O)=O
butane-2,3-diyl dimethanesulfonate
CC1Oc2cc(-c3ccc(F)cc3)nn2C1C
6-(4-fluorophenyl)-2,3-dimethyl-2,3-dihydropyrazolo[5,1-b][1,3]oxazole
المردود 71.8%

المذيبات

ظروف التفاعل

درجة الحرارة
60°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىprepared
  2. 2
    أخرىat room temperature
  3. 3
    استخلاصextracted with ethyl acetate
  4. 4
    تجفيفThe organic layer was dried over anhydrous sodium sulphate
  5. 5
    تركيزconcentrated
  6. 6
    أخرىto get the crude product
  7. 7
    أخرىPurification by column chromatography over silica gel (eluent 5-10% ethyl acetate in petrol ether)

الإجراء التجريبي

To a solution of 3-(4-fluorophenyl)-1H-pyrazol-5-ol (3 g, 16.8 mmol) in DMF (15 mL) was added K2CO3 (9.3 g, 67.4 mmol) and butane-2,3-diyl dimethanesulfonate (4.8 g, 18.5 mmol) (prepared as described in US2010/41748) at room temperature and then stirred for 16 h at 60° C. Thereafter, the reaction mixture was diluted with cold water and extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulphate and concentrated to get the crude product. Purification by column chromatography over silica gel (eluent 5-10% ethyl acetate in petrol ether) yielded 6-(4-fluorophenyl)-2,3-dimethyl-2,3-dihydropyrazolo[5,1-b][1,3]oxazole (2.8 g, 71%) as yellow oil and a mixture of diastereoisomers.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09023844B2uspto-grants-2015_05