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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 456111생성일: 2026년 10월 25일

3-Amino-2-oxazolidinone → 3-[(E)-1-[3-[(5,7-difluoroquinolin-6-yl)methyl]-[1,2,4]triazolo[4,3-b]pyridazin-6-yl]ethylideneamino]-1,3-oxazolidin-2-one

https://huagongshe.com/reaction/456111

반응식

참여 물질

역할이름HCID투입량
반응물3-Amino-2-oxazolidinoneHCID 65725—
반응물1-(3-((5,7-Difluoroquinolin-6-yl)methyl)-[1,2,4]triazolo[4,3-b]pyridazin-6-yl)ethanoneHCID 58190533—
생성물3-[(E)-1-[3-[(5,7-difluoroquinolin-6-yl)methyl]-[1,2,4]triazolo[4,3-b]pyridazin-6-yl]ethylideneamino]-1,3-oxazolidin-2-oneHCID 5091635086%

반응 단계

The title compound was prepared from 3-aminooxazolidin-2-one and 1-(3-((5,7-difluoroquinolin-6-yl)methyl)-[1,2,4]triazolo[4,3-b]pyridazin-6-yl)ethanone in 86% yield as white solid using the same procedure as described in the synthesis of example 40. 1H-NMR (400 MHz, DMSO-d6) δ ppm 9.00 (d, 1H), 8.50 (d, 1H), 8.33 (d, 1H); 7.87 (d, 1H), 7.75 (d, 1H), 7.63 (dd, 1H), 4.81 (s, 2H), 4.49 (t, 2H), 4.05 (t, 2H), 2.33 (s, 3H). LCMS (method A): [MH]+=424, tR=4.54 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08497368B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-8dcb8f2c2aeb4651875ea5a2ea5791df
출처 메모uspto-grants-2013_07