Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 3-Nitrobenzaldehyde | HCID 7449 | — |
| Reactant | Ethyl Acetoacetate | HCID 8868 | — |
| Reactant | (3-Trifluoromethylphenyl)urea | HCID 25712 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 58674265 | HCID 58674265 | — |
Reaction Steps
30.6 mg (0.15 mmol) N-[3-(trifluoromethyl)phenyl]urea are shaken together with 45.3 mg (0.3 mmol) 3-nitrobenzaldehyde, 39 mg (0.3 mmol) ethyl 3-oxobutanoate and 90 mg polyphosphoric acid ethyl ester [freshly prepared according to the procedure of Cava et al., J. Org. Chem. 34, 2665 (1969)] in 0.5 ml dioxan and 0.1 ml DMF at 80° C. for 18 hours. After adding 200 μl DMF, the reaction mixture is filtered and purified by preparative HPLC (column: Nucleosil 100-5 C 18 Nautilus 20 mm×50 mm, 5 μm; solvent A: acetonitrile, solvent B: water+0.1% formic acid; gradient: 0 min 10% A, 2 min 10% A, 6 min 90% A, 7 min 90% A, 7.1 min 10% A, 8 min 10% A; flow rate 25 ml/min; wavelength: 220 nm; injection volume: approx. 800 μl; number of injections: 1). The product containing fractions are combined and concentrated in vacuo.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07687510B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-76763cc5b2964a949bb6ee8989e08159 |
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| Source note | uspto-grants-2010_03 |
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