HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1614983Generated: November 2, 2026
Potassium Carbonate → HCID 58467874, compound
https://huagongshe.com/reaction/1614983
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,4,5-Trichloropyrimidine | HCID 237259 | — |
| Reactant | tert-Butyl [5-(2-{5-(aminomethyl)-2-[(tert-butoxycarbonyl)amino]phenyl}ethyl)pyridin-3-yl]carbamate | HCID 58467865 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 58467874 | HCID 58467874 | 41.5% |
Reaction Steps
To a solution of tert-butyl [5-(2-{5-(aminomethyl)-2-[(tert-butoxycarbonyl)amino]phenyl}ethyl)pyridin-3-yl]carbamate (0.81 g, 1.8 mmol) and 2,4,5-trichloropyrimidine (0.45 g, 2.4 mmol) in N,N-dimethylformamide (10 mL) was added potassium carbonate (1.30 g, 9.37 mmol). The resultant mixture was stirred overnight at 45° C. The reaction was quenched with water. EtOAc was added and the layers were separated. The aqueous layer was extracted with EtOAc once. The combined organic layers were washed with water, and then dried (Na2SO4), filtered, and concentrated under vacuum. The crude product was purified by silica gel column chromatography to give the desired product as a white powder (0.44 g, 40%). LCMS for C28H35Cl2N6O4 (M+H)+: m/z=589.1, 591.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08765727B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-7bc2045fbc984578a59e5a05ae730c36 |
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| Source note | uspto-grants-2014_07 |
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