HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1811709Generated: November 1, 2026
Triphenylphosphine → HCID 59224675, compound
https://huagongshe.com/reaction/1811709
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2-Amino-4,6-dichloropyrimidine | HCID 65522 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Methyl 2-methoxy-4-methyl-5-(tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate | HCID 59224652 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 59224675 | HCID 59224675 | 53.3% |
Reaction Steps
2-Amino-4,6-dichloropyrimidine (246 mg, 1.5 mmol), palladium acetate (17 mg, 0.07 mmol), triphenylphosphine (59 mg, 0.22 mmol), sodium bicarbonate (168 mg, 2.0 mmol), 1,2-dimethoxyethane (2.5 ml), and water (1.0 ml) were placed in a reaction vessel. The resulting mixture was stirred at 80° C. for 10 minutes. A 1,2-dimethoxyethane (2.5 ml) solution of 2-methoxy-4-methyl-5-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)benzoic acid methyl ester (294 mg, 1.0 mmol) obtained in Step 3 above was added dropwise to the mixture. The resulting mixture was stirred at 80° C. for 14 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-methoxy-4-methylbenzoic acid methyl ester (Compound 1-2) (164 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-8cd02d85dc874fe6af22bc722f87e0c6 |
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| Source note | uspto-grants-2013_01 |
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