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HCID 178490494, compound → HCID 178489873, compound

HRID 403461
Notes
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Reaction equation

HRID 403461 reaction equation
[OH:1][C:2]1[C:7]([NH:8][C:9](=O)[C:10]2[CH:15]=[C:14]([CH3:16])[C:13]([O:17][CH3:18])=[C:12]([CH3:19])[CH:11]=2)=[C:6]([OH:21])[N:5]=[C:4]([S:22][CH3:23])[N:3]=1>P(Cl)(Cl)(Cl)=O>[CH3:18][O:17][C:13]1[C:12]([CH3:19])=[CH:11][C:10]([C:9]2[O:21][C:6]3[N:5]=[C:4]([S:22][CH3:23])[N:3]=[C:2]([OH:1])[C:7]=3[N:8]=2)=[CH:15][C:14]=1[CH3:16]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 1

HCID 178490494HCID 178490494, compound

Product 1

HCID 178489873HCID 178489873, compoundYield 61.7%

Reagents, catalysts & solvents 1

HCID 24813Phosphorus oxychlorideSolvent

Procedure

10.1 g of N-(4,6-dihydroxy-2-methylsulfanyl-pyrimidin-5-yl)-4-methoxy-3,5-dimethyl-benzamide in 55 ml of phosphorus oxychloride were heated to 60° C. for 3 h. After cooling, the resulting solid was collected by filtration with suction and washed with methyl tert-butyl ether. The solid was then dissolved in a mixture of dichloromethane and tetrahydrofuran, washed with a saturated aqueous sodium hydrogencarbonate solution, dried and concentrated in vacuo. 5.9 g of the title compound were obtained.

Workup

temperature
After cooling
  • filtrationthe resulting solid was collected by filtration with suction
  • washwashed with methyl tert-butyl ether
  • dissolutionThe solid was then dissolved in a mixture of dichloromethane and tetrahydrofuran
  • washwashed with a saturated aqueous sodium hydrogencarbonate solution
  • customdried
  • concentrationconcentrated in vacuo
  • Sources & evidence

    ORD record
    ord-95bb604427874cce8fe38a4875d6d1d9
    Source dataset
    uspto-grants-2014_06
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US08748436B2

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes