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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 634834생성일: 2026년 10월 24일

2-Chloroimidazoline sulfate → 2-[4-(1-Isopropylaminocarbonylpiperidin-4-ylmethyl)-phenyl]amino-imidazoline

https://huagongshe.com/ko/reaction/634834

반응식

참여 물질

역할이름HCID투입량
반응물2-Chloroimidazoline sulfateHCID 12503398—
반응물4-(1-Isopropylaminocarbonylpiperidin-4-ylmethyl)-phenylamineHCID 21876857—
용매IsopropanolHCID 3776—
생성물2-[4-(1-Isopropylaminocarbonylpiperidin-4-ylmethyl)-phenyl]amino-imidazolineHCID 2187680859.2%

반응 단계

A mixture of 4-(1-isopropylaminocarbonylpiperidin-4-ylmethyl)-phenylamine (0.64 g, 2.31 mmol) and 2-chloro-2-imidazoline sulfate (0.70 g, 3.47 mmol) in 2-propanol (20 mL) was heated under reflux for 30 minutes. The reaction mixture was concentrated in vacua. The residue was diluted with water, basified with 10% sodium hydroxide solution and extracted into dichloromethane. The organic layer was washed with water and brine, dried (Na2SO4), and concentrated in vacua. The crude product was chromatographed on neutral aluminum oxide, eluting with 5% methanol/dichloromethane, and crystallized from ethyl acetate containing some ethanol, to give 2-[4-(1-isopropylaminocarbonylpiperidin-4-ylmethyl)-phenyl]amino-imidazoline (0.47 g, 59%) as a white solid, m.p. 191-192° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06184242B2
출처 데이터셋uspto-grants-2001_02
ORD IDord-defd4999d63849a5a49cf176ccee5808
출처 메모uspto-grants-2001_02