HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 250070Generated: October 29, 2026
Methanol → 6-(Pyridin-3-yl)pyrimidin-4-amine
https://huagongshe.com/reaction/250070
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-Amino-6-chloropyrimidine | HCID 238012 | — |
| Reactant | 3-Pyridinylboronic acid | HCID 2734378 | — |
| Catalyst | Dichlorobis(triphenylphosphine)palladium | HCID 6102075 | — |
| Solvent | Dimethoxyethane ethanol water | HCID 86587095 | — |
| Product | Ammonium hydroxide ethyl acetate | HCID 21904419 | — |
| Product | 6-(Pyridin-3-yl)pyrimidin-4-amine | HCID 57476574 | 79% |
Reaction Steps
A mixture of 6-chloropyrimidin-4-amine (0.324 g, 2.5 mmol), pyridin-3-ylboronic acid (0.384 g, 3.13 mmol), Na2CO3 (0.795 g, 7.50 mmol) and bis(triphenylphosphine)palladium(II)chloride (0.035 g, 0.050 mmol) was suspended in a mixture of DME/EtOH/water. The mixture was heated in the microwave synthesizer at 125° C. for 20 min and concentrated. The residue was purified by silica gel chromatography (10-60% ethyl acetate in hexanes, then 5-25% 9:1 methanol:ammonium hydroxide-ethyl acetate) to afford 6-(pyridin-3-yl)pyrimidin-4-amine (0.17 g, 0.987 mmol, 40% yield) as an off-white solid. LCMS R.T.=0.31;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07863291B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-ba40fe69a51840aab0244736e8695f2d |
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| Source note | uspto-grants-2011_01 |
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