HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1257818Generated: October 27, 2026
Sodium Carbonate → Tert-butyl 4-(2-aminopyrimidin-5-yl)benzoate
https://huagongshe.com/reaction/1257818
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-Amino-5-bromopyrimidine | HCID 231310 | — |
| Reactant | (4-((Tert-butoxy)carbonyl)phenyl)boronic acid | HCID 2773301 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Tert-butyl 4-(2-aminopyrimidin-5-yl)benzoate | HCID 67225251 | 86.6% |
Reaction Steps
Sodium carbonate (0.636 g, 6.0 mmol) in water (2.0 mL) was added to a mixture of 5-bromopyrimidin-2-amine (0.348 g, 2.0 mmol), [4-(tert-butoxycarbonyl)phenyl]boronic acid (0.533 g, 2.4 mmol) and tetrakis(triphenylphosphine)palladium (69 mg, 0.06 mmol) in ethanol (3 mL) and toluene (3 mL). The mixture was heated at 120° C. for 3 h. After cooling to RT, the mixture was diluted with EtOAc and washed with water and brine. The organic layer was dried over Na2SO4, filtered and concentrated under reduced pressure to afford the desired product (470 mg, 86.6%) which was directly used in next step. LCMS: (M+H)=272.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08461330B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-8cdfd873ee8a44ecaacbb4a34b35256d |
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| Source note | uspto-grants-2013_06 |
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