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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1616124생성일: 2026년 10월 25일

2,4-dioxo-N-(tetrahydro-2H-pyran-2-yloxy)-1,2,3,4-tetrahydroquinazoline-7-carboxamide → N-hydroxy-2,4-dioxo-1,2,3,4-tetrahydroquinazoline-7-carboxamide

https://huagongshe.com/reaction/1616124

반응식

참여 물질

역할이름HCID투입량
반응물2,4-dioxo-N-(tetrahydro-2H-pyran-2-yloxy)-1,2,3,4-tetrahydroquinazoline-7-carboxamideHCID 86664201—
용매Acetic AcidHCID 176—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물N-hydroxy-2,4-dioxo-1,2,3,4-tetrahydroquinazoline-7-carboxamideHCID 8666420244.1%

반응 단계

A solution of 2,4-dioxo-N-(tetrahydro-2H-pyran-2-yloxy)-1,2,3,4-tetrahydroquinazoline-7-carboxamide (0.12 g, 0.39 mmol) in THF (1.6 mL), acetic acid (3.2 mL) and water (0.8 mL) was heated at 60° C. for 5 h. The mixture was concentrated to dryness. The residue was purified by preparative HPLC to afford N-hydroxy-2,4-dioxo-1,2,3,4-tetrahydroquinazoline-7-carboxamide (38 mg, 44%). LC-MS: (FA) ES+ 222; 1H NMR (400 MHz, DMSO) δ 11.42 (s, 1H), 11.40 (s, 1H), 11.28 (s, 1H), 9.21 (d, J=1.6 Hz, 1H), 7.92 (d, J=8.2 Hz, 1H), 7.52 (s, 1H), 7.44 (dd, J=8.2, 1.3 Hz, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08765773B2
출처 데이터셋uspto-grants-2014_07
ORD IDord-fbe4f929a0f24a3ba09e0aa5db55f012
출처 메모uspto-grants-2014_07