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Phosphorus oxychloride → HCID 21104341, compound

HRID 1354297
Notes
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Reaction equation

HRID 1354297 reaction equation
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[NH:9][C:10](=O)[C:11]2[C:16]([CH3:17])=[N:15][N:14]([CH3:18])[C:12]=2[N:13]=1.P(Cl)(Cl)([Cl:22])=O>>[Cl:22][C:10]1[N:9]=[C:8]([C:3]2[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=2[F:1])[N:13]=[C:12]2[N:14]([CH3:18])[N:15]=[C:16]([CH3:17])[C:11]=12
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 24813Phosphorus oxychloride2×HCID 136008000HCID 136008000, compound

Product 1

HCID 21104341HCID 21104341, compoundYield 51%

Procedure

6-(2-Fluoro-phenyl)-1,3-dimethyl-1,5-dihydro-pyrazolo[3,4-d]pyrimidin-4-one (2.0 g, 7.74 mmole) was treated with 40 ml phosphorous oxychloride and heated to reflux overnight. Removed excess phosphorous oxychloride under vacuum and added ice water to the residue. Extracted product with ethyl acetate, washed with 10% sodium carbonate, water, dried over sodium sulfate (anh) and removed solvent to give crude product. Crude product was chromatographed on silica gel column eluting with chloroform to give 1.10 g pure product (yield: 51%).

Workup

  1. temperatureheated
  2. temperatureto reflux overnight
wash
Extracted product with ethyl acetate, washed with 10% sodium carbonate, water
  • dry with materialdried over sodium sulfate (anh)
  • customremoved solvent
  • customto give crude product
  • customCrude product was chromatographed on silica gel column
  • washeluting with chloroform
  • Sources & evidence

    ORD record
    ord-7cd37d6720804bdcb12e66a2a328a9fd
    Source dataset
    uspto-grants-2007_05
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US07223766B2

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes