HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 711227Generated: October 30, 2026
Potassium Phosphate, Tribasic → (2'-Methyl-[2,4'-bipyridin]-5-yl)methanamine
https://huagongshe.com/reaction/711227
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 2-Methylpyridine-4-boronic acid | HCID 4192664 | — |
| Reactant | 5-(Aminomethyl)-2-chloropyridine | HCID 7020927 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | (2'-Methyl-[2,4'-bipyridin]-5-yl)methanamine | HCID 67208679 | — |
Reaction Steps
A mixture of (2-methylpyridin-4-yl)boronic acid 15-1 (476 mg, 3.48 mmol), (6-chloropyridin-3-yl)methanamine 18-1 (496 mg, 3.48 mmol), Pd(PPh3)4 (202 mg, 0.175 mmol) and K3PO4 (1113 mg, 5.25 mmol) in dioxane (5 mL) was stirred at 96° C. under argon overnight. After cooling to room temperature, the mixture was filtered through celite and washed with ethyl acetate. The filtrate was concentrated by rotavap and the residue subjected to silica gel column chromatography with 7% ammonia-saturated methanol in dichloromethane as eluent to give (2′-methyl-[2,4′-bipyridin]-5-yl)methanamine 18-2 as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09181235B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-d158a4e1e6714eda8406e76690313d19 |
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| Source note | uspto-grants-2015_11 |
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