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HRID 4222作成日:2026年10月24日

Piperidine-1-propylamine → N-(1-Methylethyl)-N-[2-(phenylsulfonyl)ethyl]-N'-[3-(1-piperidinyl)propyl]urea

https://huagongshe.com/ja/reaction/4222

反応式

関与物質

役割名称HCID仕込み量
反応物Piperidine-1-propylamineHCID 19049—
反応物1,1'-CarbonyldiimidazoleHCID 68263—
反応物N-(2-phenylsulfonylethyl)-2-propanamineHCID 13655034—
溶媒TetrahydrofuranHCID 8028—
生成物N-(1-Methylethyl)-N-[2-(phenylsulfonyl)ethyl]-N'-[3-(1-piperidinyl)propyl]ureaHCID 2015282827.1%

反応手順

A mixture of 5.16 g (0.0319 mole) of 1,1'-carbonyldiimidazole and 4.16 g (0.029 mole) of N-(3-aminopropyl)piperidine in 400 ml of tetrahydrofuran was stirred at room temperature for 1 hr. A solution of 6.13 g (0.027 mole) of N-[2-(phenylsulfonyl)ethyl]-2-propanamine in 50 ml of tetrahydrofuran was added, and the mixture was refluxed for 20 hr. The solvent was removed in vacuo, and the residue was dissolved in a 60/40 mixture of ether and methylene chloride, respectively. The solution was extracted with three portions of water and was dried over magnesium sulfate. The solvent was removed in vacuo to give an oil. Flash chromatography on silica gel (chloroform and methanol, gradiently eluted with methanol up to 10% methanol) gave 2.89 g (27.1%) of oil:

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-f9350ef6ad3d4d59a6d8bded0cf293e3
出典メモuspto-grants-1988_02