Reaction #657314

ord-a11bc9ea5a9443439a3775cfd7ff8d84

Reaction equation

c1ccc(-c2cc3n(n2)CCCO3)cc1
2-phenyl-6,7-dihydro-5H-pyrazolo[5,1-b][1,3]oxazine
BrBr
bromine
O=S([O-])([O-])=S.[Na+].[Na+]
sodium thiosulfate
Brc1c(-c2ccccc2)nn2c1OCCC2
3-bromo-2-phenyl-6,7-dihydro-5H-pyrazolo[5,1-b][1,3]oxazine

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Otherthe phases are separated
  2. 2
    Washthe organic phase is washed with water
  3. 3
    Dryingdried over sodium sulfate
  4. 4
    OtherThe volatiles are evaporated
  5. 5
    Filtrationthe crude product is purified by filtration over silica using
  6. 6
    workup.ADDITIONa 1:1 mixture of ethyl acetate/cyclohexane as eluent
  7. 7
    OtherAfter evaporation of the solvent 7.0 g (90%) of 3-bromo-2-phenyl-6,7-dihydro-5H-pyrazolo[5,1-b][1,3]oxazine
  8. 8
    Otherare obtained as solid

Procedure

To a solution of 2-phenyl-6,7-dihydro-5H-pyrazolo[5,1-b][1,3]oxazine (6.3 g, 0.031 mol) in 60 mL chloroform is added a solution of bromine (1 eq, 5.03 g, 0.031 mol) in 40 mL chloroform over a period of 25 min at room temperature. The resulting suspension is stirred for 4 h at room temperature. Thereafter the reaction mixture is treated with aqueous sodium thiosulfate, the phases are separated and the organic phase is washed with water and dried over sodium sulfate. The volatiles are evaporated and the crude product is purified by filtration over silica using a 1:1 mixture of ethyl acetate/cyclohexane as eluent. After evaporation of the solvent 7.0 g (90%) of 3-bromo-2-phenyl-6,7-dihydro-5H-pyrazolo[5,1-b][1,3]oxazine are obtained as solid.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09023844B2uspto-grants-2015_05