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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 374045생성일: 2026년 10월 25일

1-Heptanamine → 5-(4,5-diphenyl-1H-imidazol-2-ylthio)-N-heptylpentanamide

https://huagongshe.com/reaction/374045

반응식

참여 물질

역할이름HCID투입량
반응물1-HeptanamineHCID 8127—
반응물DicyclohexylcarbodiimideHCID 10868—
반응물1-Hydroxybenzotriazole hydrateHCID 2796029—
반응물5-[(4,5-Diphenyl-1H-imidazol-2-YL)sulfanyl]pentanoic acidHCID 18958712—
용매DimethylformamideHCID 6228—
생성물5-(4,5-diphenyl-1H-imidazol-2-ylthio)-N-heptylpentanamideHCID 281779986%

반응 단계

Part C, Method 1. To a solution of 5-(4,5-diphenyl-1H-imidazol-2-ylthio)pentanoic acid (2.0 g, 0.0057 mol) in N,N-dimethylformamide (25 mL) was added 1-hydroxybenzotriazole hydrate (0.93 g, 0.0069 mol) followed by a solution of heptylamine (1.10 mL, 0.86 g, 0.0074 mol) in N,N-dimethylformamide (10 mL). The reaction mixture was cooled to 0° and dicyclohexylcarbodiimide (1.42 g, 0.0069 mol) was added portionwise as a solid. The reaction mixture was stirred for 2 hours at 0° and then stirred for 48 hours at ambient temperature. The solids were filtered and washed with N,N-dimethylformamide. The filtrate was concentrated and the residue was chromatographed with 1:1 hexane-ethyl acetate. The resulting solid was recrystallized from acetonitrile and triturated with hexane to give 5-(4,5-diphenyl-1H-imidazol-2-ylthio)-N-heptylpentanamide (2.21 g, 0.0049 mol) as a white solid, mp 104°-106°. 1H NMR (CDCl3) δ11.6(s,1H), 7.6-7.1(m,10H), 6.1-6.0(m,1H), 3.1-2.8(m,4H), 2.2(t,2H,J=7Hz), 1.9-1.7(m,2H), 1.7-1.5(m,2H), 1.4-1.1(m,10H), 0.9(t,3H,J=8Hz).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05166214
출처 데이터셋uspto-grants-1992_11
ORD IDord-536eba3ea3654f6da17de6a80ea2cc2f
출처 메모uspto-grants-1992_11