Acetonitrile → HCID 58930961, compound

HRID 1433377Notes

Reaction equation

HRID 1433377 reaction equation
[NH2:1][C:2]1[CH:19]=[CH:18][C:5]([O:6][C:7]2[C:8]3[C:15]([CH3:16])=[C:14]([CH3:17])[NH:13][C:9]=3[N:10]=[CH:11][N:12]=2)=[CH:4][CH:3]=1.C(#N)C.[F:23][C:24]1[CH:29]=[CH:28][C:27]([N:30]=[C:31]=[O:32])=[CH:26][CH:25]=1>C1(C)C=CC=CC=1>[CH3:16][C:15]1[C:8]2[C:7]([O:6][C:5]3[CH:18]=[CH:19][C:2]([NH:1][C:31]([NH:30][C:27]4[CH:28]=[CH:29][C:24]([F:23])=[CH:25][CH:26]=4)=[O:32])=[CH:3][CH:4]=3)=[N:12][CH:11]=[N:10][C:9]=2[NH:13][C:14]=1[CH3:17]

Participants

5

Reactant 3

HCID 6342AcetonitrileHCID 709554-Fluorophenyl isocyanateHCID 58931289HCID 58931289, compound

Product 1

HCID 58930961HCID 58930961, compound

Reagents, catalysts & solvents 1

HCID 1140TolueneSolvent

Procedure

4-(4-Aminophenoxy)-5,6-dimethyl-7H-pyrrolo[2,3-d]-pyrimidine was dissolved in toluene (16 mg) (0.8 ml) and acetonitrile (0.5 ml) under reflux, and then 4-fluorophenyl isocyanate (7.9 μM) was added. The mixture was stirred for 1 hour and returned to room temperature, and then the reaction system was concentrated, diethyl ether was added to the residue, and the resulting crystals were filtered out. The crystals were washed with diethyl ether to obtain the title compound (5 mg).

Workup

  1. customreturned to room temperature
  2. concentrationthe reaction system was concentrated
  3. additiondiethyl ether was added to the residue
  4. filtrationthe resulting crystals were filtered out
  5. washThe crystals were washed with diethyl ether

Sources & evidence

ORD record
ord-773749dbb4354986af4cdaaaeb5e7cd4
Source dataset
uspto-grants-2009_11
Patent number
US07612092B2

Reaction notes

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