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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 576728생성일: 2026년 10월 25일

Water → (S)-tert-butyl 6-methyl-8-oxo-3-(pyrazin-2-yl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazine-7(8H)-carboxylate

https://huagongshe.com/reaction/576728

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물AcetonitrileHCID 6342—
반응물Sodium periodateHCID 23667635—
반응물HCID 90402323HCID 90402323—
촉매Ruthenium dioxide hydrateHCID 16211523—
용매ChloroformHCID 6212—
생성물(S)-tert-butyl 6-methyl-8-oxo-3-(pyrazin-2-yl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazine-7(8H)-carboxylateHCID 9040228448%

반응 단계

To a solution of (S)-tert-butyl 6-methyl-3-(pyrazin-2-yl)-5,6-dihydro-[1,2,4]triazolo[4,3-a]pyrazine-7(8H)-carboxylate (1.0 g, 3.2 mmol) in chloroform (12 mL) was added acetonitrile (12 mL), water (30 mL), sodium metaperiodate (3.2 g, 14.9 mmol) and ruthenium (IV) oxide hydrate (62 mg, 0.4 mmol) and the reaction mixture was vigorously stirred for 30 minutes. The reaction mixture was filtered through celite, extracted with DCM, the organic layers were washed with brine, dried with Na2SO4, filtered, concentrated and purified by flash column chromatography (0-100% EtOAc in hexanes) to provide the desired compound (0.50 g, 48%). 1H NMR (400 MHz, DMSO) δ 9.47 (s, 1H), 8.83 (s, 2H), 5.01-4.92 (m, 1H), 4.89-4.79 (m, 1H), 4.73-4.66 (m, 1H), 1.52 (s, 9H), 1.21 (d, J=6.8 Hz, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09040534B2
출처 데이터셋uspto-grants-2015_05
ORD IDord-bbda560bdc494c7ebfbdc40ecca4a45b
출처 메모uspto-grants-2015_05