반응 #1979532

ord-e13c1c7baa134d909766612cd2bff277

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타as described in the synthesis of example 22

실험 절차

The title compound was prepared from 1-(1-(quinolin-6-ylmethyl)-1H-[1,2,3]triazolo[4,5-b]pyrazin-6-yl)ethanone (22.4) and 2-(aminooxy)ethanol in 21% yield using the same procedure as described in the synthesis of example 22. 1H-NMR (400 MHz, CD2Cl2) δ ppm 9.40 (s, 1H), 8.91 (m, 1H), 8.18 (d, 2H), 7.95 (d, 1H), 7.85 (dd, 1H), 7.45 (dd, 1H), 6.13 (s, 2H), 4.46 (t, 2H), 3.97 (t, 2H), 2.39 (s, 3H). LCMS (method A): [MH]+=364, tR=4.28 min.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08507676B2uspto-grants-2013_08