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HRID 1729610作成日:2026年10月27日

Methanol → 2-Thioadenosine

https://huagongshe.com/reaction/1729610

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物Carbon DisulfideHCID 6348—
反応物5-amino-1-beta-D-ribofuranosylimidazole-4-carboxamide O-ethyl-oximeHCID 53763093—
生成物2-ThioadenosineHCID 6451965—

反応手順

0.45 g of 5-amino-1-β-D-ribofuranosylimidazole-4-carboxamide O-ethyl-oxime was dissolved in 8 ml of an aqueous solution containing 7 ml of methanol, and 2 ml of carbon disulfide was added to the solution. The resulting mixture was allowed to react in an autoclave at 120° C for 6 hours under autogenous pressure (about 10 Kg/cm2). The reaction mixture was concentrated to dryness, and the residue was dissolved in water. The aqueous solution was adjusted to a pH of 2 with hydrochloric acid, and the crystals thus precipitated were filtered to obtain 2-thioadenosine, which was then dissolved in aqueous ammonia, filtered and again adjusted to a pH of 2 with hydrochloric acid to obtain 0.355 g of pure 2-thioadenosine having a melting point of 199° C (with decomposition) in a 75% yield.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US03989682
出典データセットuspto-grants-1976_11
ORD IDord-75e78e4fc27e4e2cb3ac6078bb8e2e6a
出典メモuspto-grants-1976_11