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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromo-5-methylpyridineHCID 817713—
Reactanttert-butyl (3R)-3-aminopiperidine-1-carboxylateHCID 1501974—
ReactantSodium t-butoxideHCID 23676156—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
CatalystBrettphosHCID 25112535—
Solvent1,4-DioxaneHCID 31275—
Product(R)-tert-butyl 3-((4-methylpyridin-2-yl)amino)piperidine-1-carboxylateHCID 2638504980%

Reaction Conditions

Temperature70 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260441B2
Source datasetuspto-grants-2016_02
ORD IDord-f6c70b95df2e4aae857d4835ec7edd4f
Source noteuspto-grants-2016_02