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HRID 35473作成日:2026年10月25日

Sodium Hydroxide → 5,5,7,7-tetramethylindeno[5,6-d)-imidazol-6(1H)-one

https://huagongshe.com/reaction/35473

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)-3,5-dimethyl-4-methoxypyridine hydrochlorideHCID 11694258—
反応物HCID 178429018HCID 178429018—
溶媒WaterHCID 962—
生成物5,5,7,7-tetramethylindeno[5,6-d)-imidazol-6(1H)-oneHCID 86742393—

反応手順

18.0 g (69.2 mmol) of 5,7-dihydro-2 -mercapto-5,5,7,7-tetramethylindeno[5,6-d]imidazol-6(1H)-one are suspended in 400 ml of alcohol and treated with 15.6 g (70.2 mmol) of 2-(chloromethyl)-4-methoxy-3,5-dimethylpyridine hydrochloride while cooling with ice. Thereafter, a solution of 5.6 g of sodium hydroxide in 150 ml of water is added dropwise thereto, the mixture is left to boil at reflux overnight and subseguently evaporated to dryness in vacuo. The residue is dissolved in 1000 ml of methylene chloride; the solution is washed firstly with 500 ml of 1.5N sodium hydroxide solution and then with 3×500 ml of water, dried over sodium sulphate and evaporated in vacuo. The crude product is purified on 300 g of silica gel with ethyl acetate/methylene chloride (1:1) as the elution agent. Crystallization from methylene chloride/petroleum ether gives 5,7-dihydro-2-[[(4-methoxy-3,5 -dimethyl-2ether -pyridyl)methyl]thio]-5,5,7,7 -tetramethylindeno[5,6-d)-imidazol-6(1H)-one of melting point 166°-168°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04766133
出典データセットuspto-grants-1988_08
ORD IDord-059069ab2df540db82f1bfa4253558e8
出典メモuspto-grants-1988_08