반응 #66893

ord-44264225071e46b2b14ad467f5a1d9c5

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타to yield 40 mg (32%)

실험 절차

The compound was synthesized in analogy to Example 122 from 2,4-difluoro-5-(5,6,7,8-tetrahydropyrido[4′,3′:4,5]thieno[2,3-d]pyrimidin-4-ylamino)phenol hydrochloride from Example 71A (100 mg, 0.27 mmol) and (2E)-4-(dimethylamino)but-2-enoic acid hydrochloride from Example 1A (63 mg, 0.38 mmol) to yield 40 mg (32%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08524722B2uspto-grants-2013_09