Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 27842생성일: 2026년 10월 25일
N-Isopropylpropane-1,3-diamine → N-[3-(isopropylamino)propyl]-N'-(5-chloro-2-methylphenyl)urea hydrochloride
https://huagongshe.com/reaction/27842
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | N-Isopropylpropane-1,3-diamine | HCID 76888 | — |
| 반응물 | 5-Chloro-2-methylphenyl isocyanate | HCID 2769632 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | N-[3-(isopropylamino)propyl]-N'-(5-chloro-2-methylphenyl)urea hydrochloride | HCID 20526049 | — |
반응 단계
A solution of 16.7 g. of 2-methyl-5-chlorophenylisocyanate and 50 ml. of dichloromethane was added to a stirred, cooled solution of 35 g. of N-isopropyl-1,3-diaminopropane and 250 ml. of dichloromethane. The temperature was kept at -5° to 0° C. during addition. Stirring was continued at room temperature for 20 minutes. The precipitated solid was separated by filtration. The filtrate was extracted with water, then with 200 ml. of 15% hydrochloric acid (v/v). The acid extract was made basic with saturated sodium carbonate solution, then extracted with dichloromethane. The dichloromethane solution was dried over magnesium sulfate, then evaporated to dryness. The residue was dissolved in ethanol and saturated with hydrogen chloride. The solution was evaporated to dryness in vacuo. The residue was triturated with ether until it solidified. The solid was recrystallized from EtOH/Et2O to obtain N-[3-(isopropylamino)propyl]-N'-(5-chloro-2-methylphenyl)urea hydrochloride, m.p. 180°-183° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04224242 |
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| 출처 데이터셋 | uspto-grants-1980_09 |
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| ORD ID | ord-5c47f241818b43ccbfbf009fa7869e50 |
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| 출처 메모 | uspto-grants-1980_09 |
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