تفاعل #47916

ord-64a519433fd6480c910ed37c1624e2a0

معادلة التفاعل

FC(F)(F)c1ccc(Nc2ncnc3c2CNCC3)cc1
N-(4-(Trifluoromethyl)phenyl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-4-amine
Cc1ccccc1B(O)O
o-tolylboronic acid
CCN(CC)CC
triethylamine
Cc1ccccc1N1CCc2ncnc(Nc3ccc(C(F)(F)F)cc3)c2C1
desired compound
المردود 5.0%
Cc1ccccc1N1CCc2ncnc(Nc3ccc(C(F)(F)F)cc3)c2C1
N-(4-(Trifluoromethyl)phenyl)-5,6,7,8-tetrahydro-6-o-tolylpyrido[4,3-d]pyrimidin-4-amine
المردود 5.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىthe solvent was removed under a vacuum
  2. 2
    أخرىThe residue was purified

الإجراء التجريبي

N-(4-(Trifluoromethyl)phenyl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidin-4-amine (100 mg, 0.34 mmol) was dissolved in anhydrous THF (2 mL). To the mixture was added o-tolylboronic acid (92 mg, 0.68 mmol), Cu(OAc)2 (124 mg, 0.68 mmol) and triethylamine (0.68 g, 0.095 mL). The mixture was agitated for 6 h and the solvent was removed under a vacuum. The residue was purified using a gradient of ethyl acetate:hexane (0-100%) to give the desired compound as reddish powder (6.0 mg, 5%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07745451B2uspto-grants-2010_06