Ethyl Acetate → 4-(Pyrimidin-4-yloxy)aniline

HRID 1433367Notes

Reaction equation

HRID 1433367 reaction equation
Cl[C:2]1[N:7]=[CH:6][N:5]=[C:4]([O:8][C:9]2[CH:14]=[CH:13][C:12]([N+:15]([O-])=O)=[CH:11][CH:10]=2)[CH:3]=1.C(OCC)(=O)C>[OH-].[Pd+2].[OH-].CO>[NH2:15][C:12]1[CH:13]=[CH:14][C:9]([O:8][C:4]2[CH:3]=[CH:2][N:7]=[CH:6][N:5]=2)=[CH:10][CH:11]=1

Participants

5

Reactant 2

HCID 8857Ethyl AcetateHCID 143638504-Chloro-6-(4-nitrophenoxy)pyrimidine

Product 1

HCID 229365424-(Pyrimidin-4-yloxy)anilineYield 31.4%

Reagents, catalysts & solvents 2

HCID 9942167Palladium hydroxideCatalystHCID 887MethanolSolvent

Procedure

Palladium hydroxide (20 mg) was added to solution of 6-chloro-4-(4-nitrophenoxy)pyrimidine (300 mg) in an ethyl acetate (10 ml)-methanol (10 ml) mixed solvent, and the mixture was stirred for 13 hours at room temperature under a hydrogen atmosphere at normal pressure. The reaction solution was filtered, the filtrate was concentrated, and the residue was passed through NH silica gel (Fuji Silysia Chemical). Elution was performed with a solvent (ethyl acetate:hexane=1:2) to obtain 70 mg of 4-(4-aminophenoxy)pyrimidine. The title compound (107 mg) was obtained from the obtained 4-(4-aminophenoxy)pyrimidine (70 mg) and 4-methoxyphenyl isocyanate, in the same manner as Example 10.

Workup

  1. additionmixed solvent
  2. filtrationThe reaction solution was filtered
  3. concentrationthe filtrate was concentrated
  4. washElution

Sources & evidence

ORD record
ord-e53408c723164199af532c71a7589f9b
Source dataset
uspto-grants-2009_11
Patent number
US07612092B2

Reaction notes

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