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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 570974생성일: 2026년 10월 24일

N-(Benzyloxy)-3-methyl-4-oxo-3,4-dihydroimidazo[5,1-d][1,2,3,5]tetrazine-8-carboxamide → N-Hydroxy-3-methyl-4-oxo-3,4-dihydroimidazo[5,1-d][1,2,3,5]tetrazine-8-carboxamide

https://huagongshe.com/ko/reaction/570974

반응식

참여 물질

역할이름HCID투입량
반응물N-(Benzyloxy)-3-methyl-4-oxo-3,4-dihydroimidazo[5,1-d][1,2,3,5]tetrazine-8-carboxamideHCID 49869276—
촉매PalladiumHCID 23938—
용매N,N-dimethylformamide ethyl acetateHCID 22989253—
생성물N-Hydroxy-3-methyl-4-oxo-3,4-dihydroimidazo[5,1-d][1,2,3,5]tetrazine-8-carboxamideHCID 13598585925%

반응 단계

A solution of N-(benzyloxy)-3-methyl-4-oxo-3,4-dihydroimidazo[5,1-d][1,2,3,5]tetrazine-8-carboxamide (200 mg, 0.67 mmol) and 10% Pd/C (20 mg) in ethyl acetate:DMF (5:1) (36 mL) was put under an atmosphere of hydrogen for 3 days. The mixture was filtered through a pad of Celite™ and the filtrate was concentrated under vacuum. The residue was suspended in ethyl acetate and the precipitate was filtered and washed successively with water, ethyl acetate and diethyl ether to give the pure title compound as a pale orange solid (35 mg, 25% yield). δH (DMSO-d6): 11.2 (1H, s), 9.18 (1H, s), 8.82 (1H, s), 3.86 (3H, s).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09024018B2
출처 데이터셋uspto-grants-2015_05
ORD IDord-3d74d080c0404d81b0bf1e51b7056b7c
출처 메모uspto-grants-2015_05