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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 365804Generated: October 30, 2026

Sodium Carbonate → 3-((S)-1-Methyl-pyrrolidin-2-ylmethoxy)-5-naphthalen-1-yl-pyridine

https://huagongshe.com/reaction/365804

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant1-Naphthaleneboronic acidHCID 254532—
ReactantSodium BicarbonateHCID 516892—
Reactant3-Bromo-5-((S)-1-methyl-pyrrolidin-2-ylmethoxy)-pyridineHCID 11288721—
CatalystHCID 178418397HCID 178418397—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
Product3-((S)-1-Methyl-pyrrolidin-2-ylmethoxy)-5-naphthalen-1-yl-pyridineHCID 1042604162%

Reaction Steps

To a solution of 5-bromo-3-(1-methyl-2-(S)-pyrrolidinylmethoxy)-pyridine (272 mg, 1.00 mmol) in benzene (2.0 mL) were added aqueous sodium carbonate (2.0M, 1.0 mL), tetrakis(triphenylphosphine)palladium(0) (35 mg, 0.03 mmol) and 1-naphthaleneboronic acid (189 mg, 1.10 mmol). The reaction mixture was refluxed overnight, then cooled to room temperature. Water (2 mL) was added, and solid sodium bicarbonate was added until the aqueous layer was saturated. The mixture was extracted with EtOAc, which was dried over MgSO4, filtered and concentrated. The residue was chromatographed on a silica gel column, eluting with NH4OH/MeOH/EtOAc 0:1:9 and 1:10:90 to afford a light yellowish oil (196 mg, 62%). MS (CI/NH3) m/z 319 (M+H)+. 1H NMR (CDCl3, 300 MHz) δ 1.71-1.92 (m, 3H), 2.00-2.10 (m, 1H), 2.27-2.38 (m, 1H), 2.51 (s, 3H), 2.66-2.75 (m, 1H), 3.09-3.17 (m, 1H), 3.98-4.14 (m, 2H), 7.34-7.57 (m, 5H), 7.72-7.96 (m, 3H),8.36-8.43 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06127386
Source datasetuspto-grants-2000_10
ORD IDord-4177890660c94acf9fe5f090ffc449aa
Source noteuspto-grants-2000_10