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HRID 1817790作成日:2026年10月26日

Acetyl nitrate → 5-Nitrouracil

https://huagongshe.com/reaction/1817790

反応式

関与物質

役割名称HCID仕込み量
反応物Acetyl nitrateHCID 11557—
反応物Ethyl NitrateHCID 12259—
反応物Nitrous AcidHCID 24529—
反応物2,4(1H,3H)-Pyrimidinedione, amino-HCID 148782—
反応物Sodium NitriteHCID 23668193—
反応物Sulfuric acid, mixt. with nitric acidHCID 71777668—
反応物NaNO2 acetic acidHCID 86611488—
反応物3-nitroso-1H-pyrimidine-2,4-dioneHCID 86611489—
溶媒Acetic AcidHCID 176—
溶媒WaterHCID 962—
生成物5-NitrouracilHCID 69135—
生成物5-NitrosouracilHCID 328363—

反応手順

The 5-nitrosouracil derivatives such as compound of the formula 4 may be obtained by the nitrosylation of the aminouracil 2 using standard nitration reagents. Examples of such agents include, for example, NaNO2/AcOH, HNO3/H2SO4, N2O5/P2O5/CCl4, HONO, EtONO2, CH3COONO2 and NO2+CF3SO3− that forms the nitro or the nitrosouracil derivative. Thus, the aminouracil 2 may be dissolved in an aqueous acid, such as acetic acid and water below room temperature, such as about 10° C., and NaNO2 in water is added to the aminouracil. When the reaction is deemed complete, the volatiles are removed under reduced pressure and the residue is redissolved in a mixture of solvents. Example of such mixtures of solvents include alcohols in an organic solvent, such as absolute ethanol in DICHLOROMETHANE. The resulting mixture is heated and the hot mixture may be filtered through a filter aid such as Celite 545 to remove insoluble inorganic salts. The solvent or solvent mixtures may evaporated under reduced pressure to afford the desired 5-nitrouracil or 5-nitrosouracil such as compound 4.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07598379B2
出典データセットuspto-grants-2009_10
ORD IDord-233bf0d5a0a94d0699bfbbc82bef1539
出典メモuspto-grants-2009_10