반응 #1607038

ord-b83dba455ec94d0ea43851b52a4bfbbb

반응 조건

상세 조건
See reaction.notes.procedure_details.

실험 절차

The titled compound was synthesized from 4-chloro-3-(4H-1,2,4-triazol-3-yl)thiophen-2-amine and 2-(2-oxo-3,4-dihydro-1,5-naphthyridin-1(2H)-yl)acetic acid via protocol A. LCMS method [4], retention time=1.035; MS(ESI) 389.1 (MH+, 35Cl).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US09073891B2uspto-grants-2015_07