戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1682136作成日:2026年10月24日

Hydroxide → 7-demethylmitomycin A

https://huagongshe.com/ja/reaction/1682136

反応式

関与物質

役割名称HCID仕込み量
反応物HydroxideHCID 961—
反応物Mitomycin CHCID 5746—
反応物Sodium HydroxideHCID 14798—
反応物HCID 178418361HCID 178418361—
溶媒MethanolHCID 887—
生成物7-demethylmitomycin AHCID 11727393—

反応手順

Turning now to preferred conditions for the wet route, the aqueous solution of 7-salt oxide-9a-methoxymitosane (7-Na+O- -9a-methoxymitosane when aqueous sodium hydroxide is the hydroxide solution reacted with mitomycin C) is reacted directly with acid. While aqueous acid solutions or strong acid cation exchange resin in the hydrogen form can be used as the acidifying agent, in this case, unlike in the dry route, aqueous acid solution is preferred over cation exchange resin since use of cation exchange resin requires a resin separation step whereas the water introduced with aqueous acid does not need to be removed for reaction of diazodiphenylmethane with 7-hydroxy-9a-methoxymitosane. The reaction is readily carried out, for example, by combining diphenyldiazomethane solution with the 7-salt oxide-9a-methoxymitosane solution, adjusting the pH into the desired range of about 4 to 7 with acid solution, preferably 5-15% phosphoric acid, maintaining the pH in said desired range by the periodic addition of acid solution while maintaining the temperature in the range of 0° C. to 30° C. and adding additional diphenyldiazomethane solution if needed. As previously indicated methanol is preferably used in combination with methylene chloride reaction solvent. The methanol aids in extracting formed 7-hydroxy-9a-methoxymitosane from aqueous phase for reaction in the organic phase with diazodiphenylmethane.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05175303
出典データセットuspto-grants-1992_12
ORD IDord-69ef66cecedf4868a80aa55af9583baa
出典メモuspto-grants-1992_12