Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 10884647 | HCID 10884647 | — |
| Reactant | ethyl (4-{4-[(4-{[(4-formyl-1-phenyl-1H-pyrazol-3-yl)oxy]methyl}-2-methoxyphenoxy)methyl]-5-methyl-1,3-oxazol-2-yl}phenyl)acetate | HCID 86605875 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 86605929 | HCID 86605929 | 11.3% |
Reaction Steps
A mixture of ethyl (4-{4-[(4-{[(4-formyl-1-phenyl-1H-pyrazol-3-yl)oxy]methyl}-2-methoxyphenoxy)methyl]-5-methyl-1,3-oxazol-2-yl}phenyl)acetate (1.60 g), [(2-isopropyl-1,3-thiazol-4-yl)methyl]triphenylphosphonium chloride (1.7 g), potassium carbonate (0.57 g) and N,N-dimethylformamide (30 mL) was stirred at room temperature for 17 hrs. Water was poured into the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated. The residue was subjected to silica gel column chromatography, and eluted with ethyl acetate-hexane (1:4, v/v) to give ethyl {4-[4-({4-[({4-[(Z)-2-(2-isopropyl-1,3-thiazol-4-yl)ethenyl]-1-phenyl-1H-pyrazol-3-yl}oxy)methyl]-2-methoxyphenoxy}methyl)-5-methyl-1,3-oxazol-2-yl]phenyl}acetate as colorless crystals (0.22 g, yield 11%). Recrystallization from ethyl acetate-hexane gave colorless prism crystals. melting point: 126-127° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07368578B2 |
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| Source dataset | uspto-grants-2008_05 |
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| ORD ID | ord-8a2b5489e1f248b9ad35bcbaf4e74d80 |
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| Source note | uspto-grants-2008_05 |
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