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HRID 1678323生成日期:2026年10月23日

5-对硝基苯基糠醛 → 3-(3-((5-(4-Nitrophenyl)furan-2-yl)methylene)-3,4,5,6-tetrahydropyridin-2-yl)pyridine

https://huagongshe.com/zh-CN/reaction/1678323

反应方程式

参与物

角色名称HCID投料
反应物5-对硝基苯基糠醛HCID 81567—
反应物3-(5-Ammoniopentanoyl)pyridinium chlorideHCID 67337657—
溶剂异丙醇HCID 3776—
产物3-(3-((5-(4-Nitrophenyl)furan-2-yl)methylene)-3,4,5,6-tetrahydropyridin-2-yl)pyridineHCID 6733914336.6%

反应条件

温度80 °C

反应步骤

3-(5-Ammoniopentanoyl)pyridinium chloride (95 mg, 0.38 mmol) and 5-(4-nitrophenyl)furfural (99 mg, 0.46 mmol) were combined in a reaction vessel and treated with isopropanol (6 mL). The reaction vessel was sealed and the reaction was heated to 80° C. with stirring overnight. The reaction was then cooled to room temperature, concentrated under reduced pressure and treated with saturated NaHCO3(aq). This mixture was then extracted three times with EtOAc. The EtOAc extracts were washed with brine, combined, dried over Na2SO4, filtered and concentrated under reduced pressure. The recovered material was eluted through a 20 gram column of silica gel with 10.5:7:7:1:0.1 hexane:MtBE:CH2Cl2:MeOH:NH4OH (1 liter). One sample was recovered that appeared to be highly crystalline. This material was re-crystallized from hot methanol. The crystals were recovered by vacuum filtration, washed with isopropanol then dried under vacuum giving 50 mg (36%) of an orange crystalline solid. LC-MS: RT=5.16 min, [M+H]+=360.0.

来源与证据

DOI10.6084/m9.figshare.5104873.v1
专利号US08008499B2
来源数据集uspto-grants-2011_08
ORD IDord-c61eacb8a004462aac695b8c1fa180f0
来源说明uspto-grants-2011_08