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HRID 1002作成日:2026年10月23日

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

https://huagongshe.com/ja/reaction/1002

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物4-(O-Benzylhydroxylamino)-3-methoxy-2-methylpyridineHCID 15279358—
反応物3,3-Dimethyl-9-tosyloxy-1,5-dioxaspiro[5.5]undecaneHCID 19694029—
反応物HCID 178418361HCID 178418361—
溶媒Dimethyl SulfoxideHCID 679—
溶媒TetrahydrofuranHCID 8028—
生成物4-[O-Benzyl-N-(3,3-dimethyl-1,5-dioxaspiro[5.5]undec-9-yl)hydroxylamino]-3-methoxy-2-methylpyridineHCID 19693982—

反応条件

温度50 °C

反応手順

7.3 g of 4-(O-benzylhydroxylamino)-3-methoxy-2-methylpyridine in 30 ml of absolute DMSO are deprotonated under N2 using 0.9 g of sodium hydride (80% strength). After evolution of hydrogen has ended, 11.7 g of 3,3-dimethyl-9-tosyloxy-1,5-dioxaspiro[5.5]undecane are added in 50 ml of absolute THF. The mixture is stirred at room temperature for 1 hour and at 50° C. for 4 hours. The THF is then distilled off in vacuo and the mixture is poured into water. After extracting with methylene chloride, the product is purified by chromatography on silica gel (ethyl acetate). 6.5 g=51%

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-a05cf5e0c43f4ae0a2ddb5d7e074dffb
出典メモuspto-grants-1998_03