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HRID 1415408作成日:2026年10月27日

2-(Methylamino)ethanol → Rifamycin

https://huagongshe.com/reaction/1415408

反応式

関与物質

役割名称HCID仕込み量
反応物2-(Methylamino)ethanolHCID 8016—
反応物Rifamycin SHCID 6436726—
溶媒1,4-DioxaneHCID 31275—
生成物RifamycinHCID 6324616—

反応手順

10 g (0.13 mol) of N-methylethanolamine are added to a solution of 21 g (0.03 mol) of rifamycin-S in 20 ml of dioxan and the whole heated for 15 minutes on a boiling water bath. The batch is then evaporated to dryness in vacuo and the residue chromatographed on 2kg of silica gel, using chloroform as eluant. In addition to a dark-colored head zone, two strong, yellow-colored bands are observed. The eluate of the more slowly eluted band is evaporated and the residue crystallized from aqueous methanol. After three crystallizations from aqueous methanol there is obtained 3-N-methylethanol-amino)-rifamycin-SV in the form of coarse prisms melting at 218° C (with decomposition.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04005077
出典データセットuspto-grants-1977_01
ORD IDord-c4a699024f8f439d8291345532d8ac06
出典メモuspto-grants-1977_01