반응 #69007

ord-65f397ec3e8d46fcb30e760fe36cae26

반응 방정식

COc1ccnc(Cl)n1
2-chloro-4-methoxypyrimidine
Cc1ncn(-c2ccc(N)cc2)n1
4-(3-methyl-1H-1,2,4-triazol-1-yl)aniline
COc1ccnc(Nc2ccc(-n3cnc(C)n3)cc2)n1
4-methoxy-N-(4-(3-methyl-1H-1,2,4-triazol-1-yl)phenyl)pyrimidin-2-amine

반응 조건

온도
75°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도cooled
  2. 2
    기타The layers were separated
  3. 3
    추출the aqueous layer was extracted with EtOAc (4×)
  4. 4
    건조The combined organics were dried (MgSO4)
  5. 5
    농축concentrated
  6. 6
    기타to give a near colorless solid which
  7. 7
    기타was used without further purification

실험 절차

To a solution 2-chloro-4-methoxypyrimidine (2 g, 13.8 mmol) in ethoxyethanol (50 mL) was added 4-(3-methyl-1H-1,2,4-triazol-1-yl)aniline (1.7 g, 10.6 mmol). The reaction was warmed to 75° C. for 16 h, cooled, and diluted with water and EtOAc. The layers were separated, and the aqueous layer was extracted with EtOAc (4×). The combined organics were dried (MgSO4), and concentrated to give a near colorless solid which was homogeneous by analytical HPLC analysis and was used without further purification.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08530480B2uspto-grants-2013_09