Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2-Amino-4,6-dichloropyrimidine | HCID 65522 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 59224645 | HCID 59224645 | — |
| Catalyst | Dichlorobis(triphenylphosphine)palladium | HCID 6102075 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 59224651 | HCID 59224651 | 65.3% |
Reaction Steps
2-Amino-4,6-dichloropyrimidine (246 mg, 1.5 mmol), bis(triphenylphosphine) palladium dichloride (53 mg, 0.07 mmol), sodium bicarbonate (252 mg, 3.0 mmol), 1,4-dioxane (2.5 ml), and water (1.5 ml) were placed in a reaction vessel. The resulting mixture was stirred at 80° C. for 10 minutes. To this mixture, 2-Ethoxy-4-methyl-5-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)benzoic acid methyl ester (320 mg, 1.0 mmol) obtained in Step 4 above was added dropwise after dissolving in 1,4-dioxane (2.5 ml). The resulting mixture was stirred at 80° C. for 20 hours. The reaction solution was diluted with ethyl acetate (100 ml), and washed three times with water (40 ml), and then with a saturated aqueous sodium chloride solution (40 ml). The washed ethyl acetate solution was dried over anhydrous sodium sulfate (10 g). After filtration, the filtrate was concentrated under reduced pressure. The resulting crude product was purified by silica gel column chromatography (developing solvent: n-hexane:ethyl acetate=2:1) to yield 5-(2-amino-6-chloropyrimidin-4-yl)-2-ethoxy-4-methylbenzoic acid methyl ester (Compound 1-3) (210 mg) as a yellow solid material.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08362236B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-8ec7ec39009d4bae8a17115e650baecd |
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| Source note | uspto-grants-2013_01 |
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