تفاعل #66846

ord-3bb2cc15702a4fe494510c75cdb9083c

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىto yield 258 mg (64%)

الإجراء التجريبي

In analogy to Example 54A, the title compound was synthesized from 3-chloro-4-[(3-fluorobenzyl)oxy]aniline from Example 4A (180 mg, 0.72 mmol) and tert-butyl 4-chloro-3-cyano-5,8-dihydrothieno[2,3-b:5,4-c′]dipyridine-7(6H)-carboxylate (250 mg, 0.72 mmol) from Example 53A to yield 258 mg (64%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08524722B2uspto-grants-2013_09