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HRID 1058560作成日:2026年10月27日

Ammonia → Ribavirin

https://huagongshe.com/reaction/1058560

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物Methyl 1-(2,3,5-Tri-O-acetyl-beta-L-ribofuranosyl)-1,2,4-triazole-3-carboxylateHCID 10691464—
生成物RibavirinHCID 37542—

反応手順

Methyl-1-(2,3,5-tri-O-acetyl-β-L-ribofuranosyl)-1,2,4-triazole-3-carboxylate (62 g, 161 mmol) was placed in a steel bomb and treated with freshly prepared methanolic ammonia (350 ml, prepared by passing dry HCL gas into dry methanol at 0° C. until saturation) at 0° C. The steel bomb was closed and stirred at room temperature for 18 h. The steel bomb was then cooled to 0° C., opened and the content evaporated to dryness. The residue was treated with dry ethanol (100 ml) and evaporated to dryness. The residue obtained was triturated with acetone to give a solid, which was filtered and washed with acetone. The solid was dried overnight at room temperature and dissolved in a hot EtOH (600 ml) and water (10 ml) mixture. The volume of the EtOH solution was reduced to 150 ml by heating and stirring on a hot plate. The hot EtOH solution on cooling provided colorless crystals, which were filtered, washed with acetone and dried under vacuum. Further concentration of the filtrate gave additional material. The total yield was 35 g (89%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06518253B1
出典データセットuspto-grants-2003_02
ORD IDord-57150076b67f4e4bb65abd2cd7f34124
出典メモuspto-grants-2003_02