Реакция #47915
ord-c5c8838fa6d540bc9becc3ac0dc4c426
Уравнение реакции
(5,6,7,8-Tetrahydro-pyrido[4,3-d]pyrimidin-4-yl)-(4-trifluoromethylphenyl)amine
phenylboronic acid
triethylamine
→
desired compound
Выход 6.4%
N-(4-(Trifluoromethyl)phenyl)-5,6,7,8-tetrahydro-6-phenylpyrido[4,3-d]pyrimidin-4-amine
Выход 6.4%
Реактанты
Реагенты
Растворители
Условия реакции
Подробные условия
See reaction.notes.procedure_details.
Обработка
- 1Другоеthe solvent was removed under the vacuum
- 2ДругоеThe residue was purified
Методика
The (5,6,7,8-Tetrahydro-pyrido[4,3-d]pyrimidin-4-yl)-(4-trifluoromethylphenyl)amine (100 mg, 0.34 mmol) was dissolved in anhydrous THF (2 mL). To the mixture was added phenylboronic acid (83 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 the vacuum. The residue was purified using a gradient of ethyl acetate:hexane (0-100%) to give the desired compound as reddish powder (8.0 mg, 6.0%).