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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1775331Generated: October 28, 2026

3-Bromo-5-methylpyridine → HCID 131734733, compound

https://huagongshe.com/reaction/1775331

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromo-5-methylpyridineHCID 817713—
Reactant(3S)-(-)-3-(tert-Butoxycarbonylamino)pyrrolidineHCID 1514396—
Reactant2-Dicyclohexylphosphino-2',6'-diisopropoxybiphenylHCID 16217985—
ReactantSodium t-butoxideHCID 23676156—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 131734733HCID 13173473373%

Reaction Conditions

Temperature70 °C

Reaction Steps

A solution of 3-bromo-5-methylpyridine (138 mg, 0.892 mmol), sodium tert-butoxide (154 mg, 1.604 mmol), tert-butyl N-[(3S)-pyrrolidin-3-yl]carbamate (224 mg, 1.203 mmol) and 2-(dicyclohexylphosphino)-2′,6′-isopropoxybiphenyl (RuPhos, 37.4 mmol) in anhydrous 1,4-dioxane (7 ml) was purged with argon. Tris(dibenzylideneacetone)dipalladium (0) (Pd2(DBA)3, 73.5 mg, 0.08 mmol) was added and the mixture was stirred at 70° C. for two hours in a closed vial. After cooling to room temperature the mixture was filtered through kieselguhr and concentrated under reduced pressure. The residue was purified by column chromatography (silica, gradient from 0.5 to 7% methanol containing 7N NH3 in dichloromethane (DCM)) to afford 163 mg of a yellow solid (0.588 mmol, 73%) MS (ESI) 278.2 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260441B2
Source datasetuspto-grants-2016_02
ORD IDord-8fbe72871a1c4190953b07e5852ef6a8
Source noteuspto-grants-2016_02