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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 570973생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/570973

반응식

참여 물질

역할이름HCID투입량
반응물O-BenzylhydroxylamineHCID 102313—
반응물3-Methyl-4-oxo-3,4-dihydroimidazo[5,1-d][1,2,3,5]tetrazine-8-carbonyl chlorideHCID 11020238—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물N-(Benzyloxy)-3-methyl-4-oxo-3,4-dihydroimidazo[5,1-d][1,2,3,5]tetrazine-8-carboxamideHCID 4986927663%

반응 단계

O-benzylhydroxylamine (195 μL, 1.68 mmol, 2 eq.) was added to a solution of crude 3-methyl-4-oxo-3,4-dihydroimidazo[5,1-d][1,2,3,5]tetrazine-8-carbonyl chloride (200 mg, 0.84 mmol; see Arrowsmith et al., J. Med. Chem., 2002, Vol. 45, No. 25, p. 5458) in THF (6 mL) and a precipitate formed instantly. The resulting suspension was stirred for 1 hour and 30 minutes and was then poured into ice. The suspension was diluted with water and the precipitate was filtered and washed successively with water, ethyl acetate and diethyl ether to give 158 mg of the pure title compound as an off-white solid (63% yield). δH (DMSO-d6): 11.9 (1H, s), 8.85 (1H, s), 7.42-7.50 (2H, m), 7.36-7.42 (3H, m), 4.96 (2H, s), 3.88 (3H, s).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09024018B2
출처 데이터셋uspto-grants-2015_05
ORD IDord-2ba70a7f72674459abcd25cdb7b935b0
출처 메모uspto-grants-2015_05