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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Piperidine-1-propylamine | HCID 19049 | — |
| 반응물 | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| 반응물 | N-(2-phenylsulfonylethyl)-2-propanamine | HCID 13655034 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | N-(1-Methylethyl)-N-[2-(phenylsulfonyl)ethyl]-N'-[3-(1-piperidinyl)propyl]urea | HCID 20152828 | 27.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04724235 |
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| 출처 데이터셋 | uspto-grants-1988_02 |
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| ORD ID | ord-f9350ef6ad3d4d59a6d8bded0cf293e3 |
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| 출처 메모 | uspto-grants-1988_02 |
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