تفاعل #3294

ord-7c0d2f4521364c5dbc8d4b38d2935639

معادلة التفاعل

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
Cc1ccc(N)cc1
4-methylaniline
Cc1ccc(NN2C=c3cc(-c4c(Cl)cccc4Cl)c(=O)n(C)c3=NC2)cc1
6-(2,6-Dichlorophenyl)-8-methyl-3-p-tolylamino-8H-pyrido[2,3-d]pyrimidin-7-one

ظروف التفاعل

درجة الحرارة
180°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةwas heated
  2. 2
    درجة الحرارةThe resulting solution was heated for 10 minutes
  3. 3
    أخرىMuch of the excess 4-methylaniline was evaporated at reduced pressure
  4. 4
    workup.DISSOLUTIONThe remainder was dissolved in 1 mL of ethyl acetate
  5. 5
    أخرىThe crystals that separated from the dark solution
  6. 6
    ترشيحwere filtered
  7. 7
    غسيلwashed with 2 mL of ethyl acetate
  8. 8
    أخرىRecrystallization from ethyl acetate
  9. 9
    أخرىgave pure product

الإجراء التجريبي

A mixture of 0.113 g (0.29 mmol) of 6-(2,6-dichlorophenyl)-2-methanesulfonyl-8-methyl-8H-pyrido[2,3-d]pyrimidin-7-one of Example 39 and 0.50 g (4.70 mmol) of 4-methylaniline was heated, with stirring, in a 180° C. oil bath. The resulting solution was heated for 10 minutes. Much of the excess 4-methylaniline was evaporated at reduced pressure. The remainder was dissolved in 1 mL of ethyl acetate. The crystals that separated from the dark solution were filtered and washed with 2 mL of ethyl acetate and then ether; wt 0.111 g. Recrystallization from ethyl acetate gave pure product; wt 0.050 g; mp 243°-245° C.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05733914uspto-grants-1998_03