تفاعل #56912

ord-eea57b5abc9e4e88b86d78be715ab55b

معادلة التفاعل

COc1ccc(Cl)cc1-c1cc(Cl)nc(N)n1
4-chloro-6-(5-chloro-2-methoxy-phenyl)-pyrimidin-2-yl-amine
Nc1nc(Cl)cc(Cl)n1
4,6-dichloro-pyrimidin-2-yl-amine
COc1ccc(Br)cc1B(O)O
5-bromo-2-methoxy-phenyl boronic acid
COc1ccc(Br)cc1-c1cc(Cl)nc(N)n1
4-chloro-6-(5-bromo-2-methoxy-phenyl)-pyrimidin-2-yl-amine
المردود 53.0%

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

الإجراء التجريبي

Following the method described in Example 4 for the synthesis of 4-chloro-6-(5-chloro-2-methoxy-phenyl)-pyrimidin-2-yl-amine, 4,6-dichloro-pyrimidin-2-yl-amine and 5-bromo-2-methoxy-phenyl boronic acid provided 4-chloro-6-(5-bromo-2-methoxy-phenyl)-pyrimidin-2-yl-amine (53% yield).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07419984B2uspto-grants-2008_09