반응 #3293

ord-3191b5ba687c4a38ba69160188ee969d

반응 방정식

Cn1c(=O)c(-c2c(Cl)cccc2Cl)cc2cnc(S(C)(=O)=O)nc21
6-(2,6-dichlorophenyl)-2-methanesulfonyl-8-methyl-8H-pyrido[2,3-d]pyrimidin-7-one
Cn1c(=O)c(-c2c(Cl)cccc2Cl)cc2cnc(S(C)(=O)=O)nc21
6-(2,6-Dichlorophenyl)-2-methanesulfonyl-8-methyl-8H-pyrido[2,3-d]pyrimidin-7-one
NC1CCCCC1
cyclohexylamine
Cn1c(=O)c(-c2c(Cl)cccc2Cl)cc2cnc(NC3CCCCC3)nc21
2-Cyclohexylamino-6-(2,6-dichlorophenyl)-8-methyl-8H-pyrido[2,3-d]pyrimidin-7-one

반응 조건

온도
134°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도The resulting solution was heated
  2. 2
    온도at reflux for 2 minutes
  3. 3
    기타Most of the excess amine was evaporated at reduced pressure
  4. 4
    workup.DISSOLUTIONThe remaining gum was dissolved in 2 mL of ethyl acetate hot
  5. 5
    workup.ADDITIONPetroleum ether (2 mL) was added
  6. 6
    기타the crystals that separated from the cooled solution
  7. 7
    여과were filtered
  8. 8
    세척washed with water
  9. 9
    기타Recrystallization from ethyl acetate
  10. 10
    기타gave pure crystalline product

실험 절차

A mixture of 0.100 g (0.26 mmol) of 6-(2,6-dichlorophenyl)-2-methanesulfonyl-8-methyl-8H-pyrido[2,3-d]pyrimidin-7-one of Example 39 and 0.300 g (3.00 mmol) of cyclohexylamine was heated to the boiling point (134° C.). The resulting solution was heated at reflux for 2 minutes. Most of the excess amine was evaporated at reduced pressure. The remaining gum was dissolved in 2 mL of ethyl acetate hot. Petroleum ether (2 mL) was added, and the crystals that separated from the cooled solution were filtered and washed with water; wt 0.090 g. Recrystallization from ethyl acetate gave pure crystalline product; 0.048 g; mp 242°-244° C.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05733914uspto-grants-1998_03