Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 2-(2,4-dimethoxybenzylamino)acetate | HCID 19895532 | — |
| Reactant | Ethyl 4-(bromomethyl)-3-(4-methoxyphenyl)isoxazole-5-carboxylate | HCID 67529710 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | HCID 67531325 | HCID 67531325 | 56.3% |
Reaction Steps
Ethyl 4-(bromomethyl)-3-(4-methoxyphenyl)isoxazole-5-carboxylate (47.5 mmol) was dissolved in 100 mL of DMF. N-(2,4-dimethoxybenzyl)glycine ethyl ester (12.0 g, 47.5 mmol) and potassium carbonate (7.2 g, 41.6 mmol) were added, and the mixture was stirred at room temperature for 16 h. EtOAc (200 mL) and brine (200 mL) were added and the aqueous layer was extracted with additional EtOAc. The combined organic layer was washed with water and brine, and dried over MgSO4. After solvent was removed in vacuo, the crude was purified by flash chromatography (0-35% EtOAc/hexanes) to give 13.7 g of the title compound. 1H NMR (CDCl3, 200 MHz): δ=8.00 (d, 2H, J=8.8 Hz), 7.06-7.15 (m, 1H), 6.93 (d, 2H, J=8.8 Hz), 6.30-6.50 (m, 2H), 4.47 (q, 2H, J=7.4 Hz), 4.10-4.22 (m, 2H), 3.70-3.90 (m, 9H), 3.66 (s, 4H), 3.31 (s, 2H), 1.43 (t, 3H, J=7.0 Hz), 1.20-1.40 (m, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08269008B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-87542e1462cf4397a4e0e2fb8204c0f4 |
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| Source note | uspto-grants-2012_09 |
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