HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1775338Generated: October 31, 2026
3-Bromo-5-methylpyridine → (R)-tert-butyl 3-((4-methylpyridin-2-yl)amino)piperidine-1-carboxylate
https://huagongshe.com/reaction/1775338
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Bromo-5-methylpyridine | HCID 817713 | — |
| Reactant | tert-butyl (3R)-3-aminopiperidine-1-carboxylate | HCID 1501974 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Catalyst | Brettphos | HCID 25112535 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | (R)-tert-butyl 3-((4-methylpyridin-2-yl)amino)piperidine-1-carboxylate | HCID 26385049 | 80% |
Reaction Steps
3-Bromo-5-methylpyridine (200 mg, 1.163 mmol), sodium tert-butoxide (223 mg, 2.325 mmol), tert-butyl (3R)-3-aminopiperidine-1-carboxylate (349 mg, 1.744 mmol) and BrettPhos (31.2 mg, 0.058 mmol) in anhydrous dioxane (10 ml) was purged with argon. Pd2(DBA)3 (53.2 mg, 0.058 mmol) was added and the mixture was stirred at 70° C. for two hours. After cooling to room temperature the mixture was filtered through kieselguhr, the filtrate was concentrated under reduced pressure and the residue was purified by column chromatography (silica, gradient from 0.5 to 10% methanol containing 7N NH3 in DCM) to yield 271 mg of an orange solid (0.93 mmol, 64%) MS (ESI) m/z=292.2 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09260441B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-f6c70b95df2e4aae857d4835ec7edd4f |
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| Source note | uspto-grants-2016_02 |
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