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HRID 1109048作成日:2026年10月27日

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

https://huagongshe.com/reaction/1109048

反応式

関与物質

役割名称HCID仕込み量
反応物1-HeptanamineHCID 8127—
反応物DicyclohexylcarbodiimideHCID 10868—
反応物1-Hydroxybenzotriazole hydrateHCID 2796029—
反応物5-[(4,5-Diphenyl-1H-imidazol-2-YL)sulfanyl]pentanoic acidHCID 18958712—
溶媒DimethylformamideHCID 6228—
生成物5-(4,5-diphenyl-1H-imidazol-2-ylthio)-N-heptylpentanamideHCID 281779986%

反応手順

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) δ 11.6(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=7 Hz), 1.9-1.7(m,2H), 1.7-1.5(m,2H), 1.4-1.1(m,10H), 0.9(t,3H,J=8 Hz).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05318984
出典データセットuspto-grants-1994_06
ORD IDord-7c80805ee3214b939d9a933e798eae07
出典メモuspto-grants-1994_06