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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2263898생성일: 2026년 10월 27일

1-(3-(Methylsulfonyl)propyl)piperazine dihydrochloride → 2-(4-{(4S,5R)-4,5-Bis-(4-chloro-phenyl)-1-[4-(3-methanesulfonyl-propyl)-piperazine-1-carbonyl]-4,5-dimethyl-4,5-dihydro-1H-imidazol-2-yl}-3-ethoxy-phenyl)-2-methyl-propionitrile

https://huagongshe.com/reaction/2263898

반응식

참여 물질

역할이름HCID투입량
반응물1-(3-(Methylsulfonyl)propyl)piperazine dihydrochlorideHCID 49853479—
반응물rac-(4S*,5R*)-4,5-Bis-(4-chloro-phenyl)-2-[4-(cyano-dimethyl-methyl)-2-ethoxy-phenyl]-4,5-dimethyl-4,5-dihydro-imidazole-1-carbonyl chlorideHCID 72455749—
생성물2-(4-{(4S,5R)-4,5-Bis-(4-chloro-phenyl)-1-[4-(3-methanesulfonyl-propyl)-piperazine-1-carbonyl]-4,5-dimethyl-4,5-dihydro-1H-imidazol-2-yl}-3-ethoxy-phenyl)-2-methyl-propionitrileHCID 17754892—

반응 단계

In a manner analogous to the method described in example 5, rac-(4S*,5R*)-4,5-bis-(4-chloro-phenyl)-2-[4-(cyano-dimethyl-methyl)-2-ethoxy-phenyl]-4,5-dimethyl-4,5-dihydro-imidazole-1-carbonyl chloride was reacted with 1-(3-methanesulfonyl-propyl)-piperazine dihydrochloride (prepared as described in Fotouhi, N. et al. WO 2005110996) to give the title compound as a racemic mixture. The enantiomers were then separated by supercritical fluid chromatography (Berger Instrument Multi-Gram II, Daicel ChiralPak OD-H 3×25 cm, 35° C. at 100 bar, eluting with 35% methanol in carbon dioxide). LR-MS: 738.0 [(M+H)+]

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07851626B2
출처 데이터셋uspto-grants-2010_12
ORD IDord-83baff9bc9a8442a887308434599d6ee
출처 메모uspto-grants-2010_12