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HRID 745591作成日:2026年10月26日

Sodium Hydroxide → 1,8-Dihydro-2-[[(5-methyl-2-pyridyl)methyl]thio]-m-dioxino(4,5-f)benzimidazole dihydrochloride

https://huagongshe.com/reaction/745591

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物2-(Chloromethyl)-5-methylpyridine hydrochlorideHCID 23313795—
反応物HCID 178527751HCID 178527751—
溶媒WaterHCID 962—
生成物1,8-Dihydro-2-[[(5-methyl-2-pyridyl)methyl]thio]-m-dioxino(4,5-f)benzimidazole dihydrochlorideHCID 70454849—

反応手順

To 3.7 g of 1,8-dihydro-m-dioxino(4,5-f)benzimidazole-2-thiol, suspended in 60 ml of alcohol, were added dropwise while stirring 1.5 g of sodium hydroxide in 30 ml of water and, after 30 minutes, there were added 3.4 g of 5-methyl-2-chloromethylpyridine hydrochloride. The mixture was left to boil at reflux overnight, then evaporated and the residue was taken up in methylene chloride. This mixture was washed first with 3N sodium hydroxide, then neutral with water, dried over sodium sulfate and evaporated in vacuo. The crude porduct was dissolved while heating in a small amount of methanol and treated with 25 ml of 5N hydrochloric acid in ethylacetate. There was obtained 1,8-dihydro-2-[[(5-methyl-2-pyridyl)methyl]thio]-m-dioxino(4,5-f)benzimidazole dihydrochloride of melting point 153°-155° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04599347
出典データセットuspto-grants-1986_07
ORD IDord-e00a739f4fa644628b608610ef8b8b3f
出典メモuspto-grants-1986_07