HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2406087Generated: October 31, 2026
Sodium Carbonate → 5-(3,4-Dimethylphenyl)pyrimidin-2-amine
https://huagongshe.com/reaction/2406087
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 2-Amino-5-bromopyrimidine | HCID 231310 | — |
| Reactant | 3,4-Dimethylphenylboronic acid | HCID 2734348 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-(3,4-Dimethylphenyl)pyrimidin-2-amine | HCID 66586919 | — |
Reaction Steps
Into a 250-mL 3-necked round bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed 5-bromopyrimidin-2-amine (5 g, 28.74 mmol, 1.00 equiv), 3,4-dimethylphenylboronic acid (4.4 g, 29.33 mmol, 1.00 equiv), dioxane (85 mL), methanol (29 mL), sodium carbonate (6.1 g, 57.55 mmol, 2.00 equiv) in water (29 mL), and Pd(PPh3)4 (664 mg, 0.57 mmol, 0.02 equiv). The resulting solution was stirred overnight at 100° C. in an oil bath. The mixture was concentrated under vacuum. The residue was applied onto a silica gel column and eluted with dichloromethane:methanol (50:1). This resulted in 6 g (crude) of 5-(3,4-dimethylphenyl)pyrimidin-2-amine as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08809339B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-7e4c553a2e62415a95353fc7130ea34b |
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| Source note | uspto-grants-2014_08 |
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