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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1058560생성일: 2026년 10월 26일

Ammonia → Ribavirin

https://huagongshe.com/reaction/1058560

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물Methyl 1-(2,3,5-Tri-O-acetyl-beta-L-ribofuranosyl)-1,2,4-triazole-3-carboxylateHCID 10691464—
생성물RibavirinHCID 37542—

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06518253B1
출처 데이터셋uspto-grants-2003_02
ORD IDord-57150076b67f4e4bb65abd2cd7f34124
출처 메모uspto-grants-2003_02