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HRID 570973作成日:2026年10月26日

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

反応式

関与物質

役割名称HCID仕込み量
反応物O-BenzylhydroxylamineHCID 102313—
反応物3-Methyl-4-oxo-3,4-dihydroimidazo[5,1-d][1,2,3,5]tetrazine-8-carbonyl chlorideHCID 11020238—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物N-(Benzyloxy)-3-methyl-4-oxo-3,4-dihydroimidazo[5,1-d][1,2,3,5]tetrazine-8-carboxamideHCID 4986927663%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09024018B2
出典データセットuspto-grants-2015_05
ORD IDord-2ba70a7f72674459abcd25cdb7b935b0
出典メモuspto-grants-2015_05