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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570973Generated: October 26, 2026

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

https://huagongshe.com/reaction/570973

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-BenzylhydroxylamineHCID 102313—
Reactant3-Methyl-4-oxo-3,4-dihydroimidazo[5,1-d][1,2,3,5]tetrazine-8-carbonyl chlorideHCID 11020238—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductN-(Benzyloxy)-3-methyl-4-oxo-3,4-dihydroimidazo[5,1-d][1,2,3,5]tetrazine-8-carboxamideHCID 4986927663%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09024018B2
Source datasetuspto-grants-2015_05
ORD IDord-2ba70a7f72674459abcd25cdb7b935b0
Source noteuspto-grants-2015_05