تفاعل #60768

ord-8578b14822cf4369b70e5cbd9aec395b

معادلة التفاعل

NC1=c2ccsc2=NCN1c1ccc(N)cc1
4-Amino-3-(4-aminophenyl)thieno[2,3-d]pyrimidine
[N-]=C=O
isocyanate
O=C=Nc1cc(C(F)(F)F)ccc1F
2-fluoro-5-trifluoromethyl-phenyl isocyanate
CCN(C(C)C)C(C)C
diisopropylethylamine
NC(=O)N(c1ccc(N2CN=c3sccc3=C2N)cc1)c1cc(C(F)(F)F)ccc1F
4-Amino-3-(4-((2-fluoro-5-(trifluoromethyl)phenyl)-aminocarbonylamino)phenyl)thieno[2,3-d]pyrimidine

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    تركيزconcentrated to dryness in a Speedvac system
  2. 2
    أخرىpurified by prep HPLC
  3. 3
    workup.ADDITIONThe fraction containing the desired product
  4. 4
    أخرىwas collected
  5. 5
    تركيزconcentrated to dryness

الإجراء التجريبي

4-Amino-3-(4-aminophenyl)thieno[2,3-d]pyrimidine (0.2 mmoles) was dissolved in 1 mL amine-free DMF and treated with 0.3 mmoles of the isocyanate of choice (2-fluoro-5-trifluoromethyl-phenyl isocyanate) and 0.6 mmoles of diisopropylethylamine for 2 hours at room temperature. The reaction mixture was treated with 0.5 mL 1:1 methanol-triethylamine for half an hour and concentrated to dryness in a Speedvac system, reconstituted in 1 mL DMSO and purified by prep HPLC. The fraction containing the desired product was collected and concentrated to dryness. MH+=448.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07427623B2uspto-grants-2008_09