N-methoxyl formamide-orientated method for synthesizing ferrocene and pyridone derivative
A technology for methoxy ferrocene and methoxy ferrocene carboxamide is applied in the field of ferrocene pyridone-type fused heterocyclic compounds and the synthesis thereof, and can solve problems such as difficult conversion of compounds, and achieves easy operation, chemical Unique structure
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0033] N-methoxyferrocenecarboxamide (0.1036g, 0.4mmol), diphenylacetylene (0.1424g, 0.8mmol), palladium acetate (0.0100g, 0.044mmol), sodium acetate (0.0410g, 0.5mmol), A mixture of CTAB (0.0292g, 0.08mmol) and toluene (2mL) was reacted at 65°C for 12 hours. The reaction mixture was cooled to room temperature, 5 mL of water was added, and then extracted with ethyl acetate, the extract was washed with saturated brine, the organic phase was dried over anhydrous magnesium sulfate, and the filtrate was evaporated under reduced pressure to obtain a crude product. The crude product was separated and purified by column chromatography (silica gel: 200-300 mesh, eluent: ethyl acetate / petroleum ether=1:1, v / v, R f =0.5) to obtain a red solid, N-methoxy-5,6-diphenylferroceno[c]pyridin-2(1H)-one, with a yield of 92%, m.p.177°C (dec.).
[0034] HR-MS(ESI)(m / z): Calcd.forC 26 h 21 FeNO 2 [M] + 435.0922,Found:435.0921.
[0035] 1 HNMR (300MHz, CDCl 3 ):δ7.24-7.21(m,10H),5.32(d,1H,J=...
Embodiment 2
[0037] N-methoxyferrocenecarboxamide (0.1036g, 0.4mmol), diphenylacetylene (0.1424g, 0.8mmol), palladium acetate (0.0100g, 0.044mmol), copper acetate (0.0020g, 0.011mmol), A mixture of sodium acetate (0.0410g, 0.5mmol), CTAB (0.0292g, 0.08mmol) and toluene (2mL) was reacted at 65°C for 8 hours. The reaction mixture was cooled to room temperature, 5 mL of water was added, and then extracted with ethyl acetate, the extract was washed with saturated brine, the organic phase was dried over anhydrous magnesium sulfate, and the filtrate was evaporated under reduced pressure to obtain a crude product. The crude product was separated and purified by column chromatography (silica gel: 200-300 mesh, eluent: ethyl acetate / petroleum ether=1:1, v / v, R f =0.5) to obtain a red solid, N-methoxy-5,6-diphenylferroceno[c]pyridin-2(1H)-one, with a yield of 93%, m.p.177°C (dec.).
[0038] HR-MS(ESI)(m / z): Calcd.forC 26 h 21 FeNO 2 [M] + 435.0922,Found:435.0921.
[0039] 1 HNMR (300MHz, CDCl...
Embodiment 3
[0041] N-methoxyferrocenecarboxamide (0.1036g, 0.4mmol), 1-phenyl-2-(4-nitrophenyl) acetylene (0.1785g, 0.8mmol), palladium acetate (0.0100g, 0.044mmol ), copper acetate (0.0020g, 0.011mmol), sodium acetate (0.0410g, 0.5mmol), CTAB (0.0292g, 0.08mmol) and acetonitrile (2mL) were reacted at 65°C for 7 hours. After the reaction mixture was cooled, 5 mL of water was added first, and then extracted with ethyl acetate. The extract was washed with saturated brine, and the organic phase was dried with anhydrous magnesium sulfate. The filtrate was distilled off the solvent under reduced pressure to obtain a crude product. The crude product was separated and purified by column chromatography (silica gel: 200-300 mesh, eluent: ethyl acetate / petroleum ether=1:1, v / v, R f =0.5) to obtain a dark red solid, N-methoxy-6-phenyl-5-(4-nitrophenyl)ferrocene[c]pyridin-2(1H)-one, yield 98%, m.p.165°C (dec.).
[0042] HR-MS(ESI)(m / z): Calcd.forC 26 h 20 FeN 2 o 4 [M+H] + 481.0851, Found: 481...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com