Reaction #5910

ord-9399f232cbbb4b3389dd35141f07ec6e

Reaction equation

O=P(O)(O)O
orthophosphoric acid
[H-].[Na+]
sodium hydride
CN(C)OC(=O)c1c(O)cccc1-c1cc[nH]n1
3-pyrazolyl-2-(N,N-dimethylaminooxycarbonyl)-phenol
COc1cc(OC)nc(S(C)(=O)=O)n1
2-methylsulfonyl-4,6-dimethoxypyrimidine
COc1cc(OC)nc(Oc2cccc(-c3cc[nH]n3)c2C(=O)ON(C)C)n1
6-Pyrazolyl-2-(4,6-dimethoxypyrimidin-2-yloxy)-1-(N,N-dimethylaminooxycarbonyl)-benzene

Conditions

Temperature
30°CELSIUS
Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    workup.STIRRINGthe mixture is stirred for 12 hours at room temperature
  2. 2
    workup.ADDITIONhas previously been added
  3. 3
    Dryingdried over sodium sulfate
  4. 4
    Otherafter evaporation
  5. 5
    Otheris purified
  6. 6
    Otherto give a colorless solid

Procedure

At 10° C., 0.30 g (0.01 mol) of sodium hydride (80% strength) is added to a solution of 2.47 g (10 mmol) of 3-pyrazolyl-2-(N,N-dimethylaminooxycarbonyl)-phenol in 25 ml of anhydrous dimethylformamide, and the reaction mixture is stirred for 3 hours at 30° C. 2.18 g (0.01 mol) of 2-methylsulfonyl-4,6-dimethoxypyrimidine is added and the mixture is stirred for 12 hours at room temperature. The reaction mixture is introduced into 500 ml of water to which 2.5 ml of orthophosphoric acid has previously been added. The oil which separates out is taken up in ethyl acetate and dried over sodium sulfate. The greasy residue remaining after evaporation is purified to give a colorless solid.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05246914uspto-grants-1993_09