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HRID 4228作成日:2026年10月23日

Citric Acid → N-[2-(Diethylamino)ethyl]-N-methyl-N'-(1-methylethyl)-N'-[2-(phenylsulfonyl)ethyl]urea citrate hydrate

https://huagongshe.com/ja/reaction/4228

反応式

関与物質

役割名称HCID仕込み量
反応物Citric AcidHCID 311—
反応物TriethylamineHCID 8471—
反応物1,2-Ethanediamine, N1,N1-diethyl-N2-methyl-HCID 66034—
反応物N-(1-methylethyl)-N-[2-(phenylsulfonyl)ethyl]carbamic chlorideHCID 13655164—
溶媒MethanolHCID 887—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物N-[2-(Diethylamino)ethyl]-N-methyl-N'-(1-methylethyl)-N'-[2-(phenylsulfonyl)ethyl]urea citrate hydrateHCID 70419038—

反応手順

A mixture of 6.65 g (0.023 mole) of N-(1-methylethyl)-N-[2-(phenylsulfonyl)ethyl]carbamic chloride; 3.0 g (0.023 mole) of N,N-diethyl-N'-methylethylenediamine and triethylamine (2.7 g, 0.0267 mole) in 400 ml of tetrahydrofuran was stirred at room temperature for 10 hr. The solvent was removed in vacuo, and the residue was dissolved in a 60/40 mixture of ether and methylene chloride. This solution was extracted with several portions of water and was dried over magnesium sulfate. The solvent was removed in vacuo to give an oil. This was dissolved in methanol, an excess of citric acid was added, and ether was added. A solid precipitated to give 11.08 g (82.4%) of white, crystalline solid; m.p. 77°-82° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04724235
出典データセットuspto-grants-1988_02
ORD IDord-1bbdfdf4f42246edb2dbfdf161a6a0b2
出典メモuspto-grants-1988_02