反应 #657309

ord-ca030abcf55f4cd2950e44fc900b0eee

反应方程式

Oc1cc(-c2ccc(F)cc2)n[nH]1
3-(4-fluorophenyl)-1H-pyrazol-5-ol
O=C([O-])[O-].[K+].[K+]
K2CO3
CS(=O)(=O)OCC(F)(F)COS(C)(=O)=O
2,2-difluoropropane-1,3-diyl dimethanesulfonate
Fc1ccc(-c2cc3n(n2)CC(F)(F)CO3)cc1
6,6-difluoro-2-(4-fluorophenyl)-6,7-dihydro-5H-pyrazolo[5,1-b][1,3]oxazine
收率 56.0%

溶剂

反应条件

温度
60°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    萃取extracted with diethyl ether
  2. 2
    干燥The organic layer was dried over anhydrous sodium sulphate
  3. 3
    浓缩concentrated
  4. 4
    其他to get the crude product
  5. 5
    其他Purification by column chromatography over silica gel (eluent 5-10% ethyl acetate in petrol ether)

实验过程

To a solution of 3-(4-fluorophenyl)-1H-pyrazol-5-ol (4 g, 22.47 mmol) in DMF (30 mL) was added K2CO3 (12.4 g, 89.88 mmol) and 2,2-difluoropropane-1,3-diyl dimethanesulfonate (9 g, 33.7 mmol) at room temperature and then stirred for 16 h at 60° C. The progress of the reaction was monitored by TLC. Thereafter, the reaction mixture was diluted with cold water and extracted with diethyl ether. 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 6,6-difluoro-2-(4-fluorophenyl)-6,7-dihydro-5H-pyrazolo[5,1-b][1,3]oxazine (3.2 g, 56%) as an off-white solid.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US09023844B2uspto-grants-2015_05