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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4222생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Piperidine-1-propylamineHCID 19049—
반응물1,1'-CarbonyldiimidazoleHCID 68263—
반응물N-(2-phenylsulfonylethyl)-2-propanamineHCID 13655034—
용매TetrahydrofuranHCID 8028—
생성물N-(1-Methylethyl)-N-[2-(phenylsulfonyl)ethyl]-N'-[3-(1-piperidinyl)propyl]ureaHCID 2015282827.1%

반응 단계

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:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04724235
출처 데이터셋uspto-grants-1988_02
ORD IDord-f9350ef6ad3d4d59a6d8bded0cf293e3
출처 메모uspto-grants-1988_02