Réaction #40359

ord-5891a95dbe0a4f5487ba99d0197a9015

Équation de réaction

CCNC
methyl ethyl amine
Cc1cc(Oc2ccnc(N(C)c3ccccc3)n2)c(C)cc1N
[4-(4-Amino-2,5-dimethyl-phenoxy)-pyrimidin-2-yl]-methyl-phenyl-amine
COC(OC)OC
trimethoxymethane
Cc1ccc(S(=O)(=O)O)cc1
p-toluene sulfonic acid
CCN(C)C=Nc1cc(C)c(Oc2ccnc(N(C)c3ccccc3)n2)cc1C
N′-{2,5-dimethyl-4-[2-(methyl-phenyl-amino)-pyrimidin-4-yloxy]-phenyl}-N-ethyl-N-methyl-formamidine

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    workup.ADDITIONwere added
  2. 2
    TempératureThe reaction mixture was refluxed for 2 hrs
  3. 3
    Concentrationconcentrated in vacuo
  4. 4
    Autrewas evaporated
  5. 5
    Autreyielded 280 mg (89%) with a purity of 87%

Mode opératoire

To a mixture of 252 mg (0.7 mmol) of [4-(4-Amino-2,5-dimethyl-phenoxy)-pyrimidin-2-yl]-methyl-phenyl-amine and 4 ml of trimethoxymethane, 20 mg of p-toluene sulfonic acid were added. The reaction mixture was refluxed for 2 hrs and concentrated in vacuo. The mixture was solved in 10 ml of dichloromethane and 62 mg (1.05 mmol) methyl ethyl amine was added. After stirring 18 hrs at ambient temperature the mixture was evaporated and yielded 280 mg (89%) with a purity of 87%; log P (pH 2.3)=1.61.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07727986B2uspto-grants-2010_06