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HRID 1004作成日:2026年10月23日

4-[O-Benzyl-N-(3,3-dimethyl-1,5-dioxaspiro[5.5]undec-9-yl)hydroxylamino]-3-methoxy-2-methylpyridine → 4-(3,3-Dimethyl-1,5-dioxaspiro[5.5]undec-9-ylamino)-3-methoxy-2-methylpyridine

https://huagongshe.com/ja/reaction/1004

反応式

関与物質

役割名称HCID仕込み量
反応物4-[O-Benzyl-N-(3,3-dimethyl-1,5-dioxaspiro[5.5]undec-9-yl)hydroxylamino]-3-methoxy-2-methylpyridineHCID 19693982—
触媒NickelHCID 935—
溶媒MethanolHCID 887—
生成物4-(3,3-Dimethyl-1,5-dioxaspiro[5.5]undec-9-ylamino)-3-methoxy-2-methylpyridineHCID 19693990—

反応手順

6.5 g of 4-[O-benzyl-N-(3,3-dimethyl-1,5-dioxaspiro[5.5]undec-9-yl)hydroxylamino]-3-methoxy-2-methylpyridine in 70 ml of methanol are hydrogenated using 2 g of Raney nickel at normal pressure until absorption of hydrogen is complete. After filtering, the filtrate is concentrated and the product is dissolved in diisopropyl ether. Crystallization takes place on addition of hexane. 4.3 g=90%; m.p.: 45° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05723450
出典データセットuspto-grants-1998_03
ORD IDord-f4dba46589654bd6a818f29b87cc4306
出典メモuspto-grants-1998_03