反応 #163519

ord-5ddbdf7a5b7e43f8b9d86a7bce001542

反応方程式

CN1C(=O)NC(Nc2nc(Cl)nc(Cl)n2)C1=O
5-(4,6-dichloro-[1,3,5]triazin-2-ylamino)-3-methyl-imidazolidine-2,4-dione
O=C([O-])[O-].[K+].[K+]
potassium carbonate
Cc1ccc(CN)cc1
4-methyl-benzylamine
Cc1ccc(CNc2nc(Cl)nc(NC3NC(=O)N(C)C3=O)n2)cc1
crude product
Cc1ccc(CNc2nc(Cl)nc(NC3NC(=O)N(C)C3=O)n2)cc1
5-[4-chloro-6-(4-methyl-benzylamino)-[1,3,5]-triazin-2-ylamino]-3-methyl-imidazolidine-2,4-dione

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他The ethyl acetate layer was separated
  2. 2
    その他dried
  3. 3
    その他evaporated

実験手順

To a stirred suspension of 5-(4,6-dichloro-[1,3,5]triazin-2-ylamino)-3-methyl-imidazolidine-2,4-dione (Example 1.3, Part D) (200 mg, 0.72 mmol) and potassium carbonate (219 mg, 1.59 mmol) in dimethylformamide (5 mL) at room temperature was added 4-methyl-benzylamine (0.1 mL, 0.79 mmol). The reaction mixture was stirred at 35° for 24 h and then diluted with water and ethyl acetate. The ethyl acetate layer was separated, dried and evaporated to give the crude product which was used directly in the next step.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08835629B2uspto-grants-2014_09