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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1780300Generated: November 2, 2026

3-Bromo-5-((S)-1-methyl-pyrrolidin-2-ylmethoxy)-pyridine → HCID 15480241, compound

https://huagongshe.com/reaction/1780300

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Bromo-5-((S)-1-methyl-pyrrolidin-2-ylmethoxy)-pyridineHCID 11288721—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
ProductHCID 15480241HCID 1548024194.3%

Reaction Steps

To a solution of 5-bromo-3-(1-methyl-2-(S)-pyrrolidinylmethoxy)-pyridine (272 mg, 1.0 mmol) in toluene (10.0 mL) was added 3-pyridinyltributyltin (442 mg, 1.2 mmol) and tetrakis(triphenylphosphine)palladium(0) (35 mg, 0.03 mmol). After being refluxed overnight, the resulting mixture was cooled to room temperature. Solvent was removed, and the residue was chromatographed on a silica gel column, eluting with NH4OH/MeOH/EtOAc 0:1:9 and 1:10:90 to afford an oil (127 mg, 48%). MS (CI/NH3) m/z 270 (M+H)+. 1H NMR (CDCl3, 300 MHz) δ1.70-1.93 (m, 3H), 2.00-2.12 (m, 1H), 2.28-2.39 (m, 1H), 2.52 (s, 3H), 2.67-2.76 (m, 1H), 3.11-3.18 (m, 1H), 3.98-4.13 (m, 2tt), 7.38-7.44 (m, 2H), 7.86-7.92 (m, 1H0, 8.37 (d, J=3.0 Hz, 1H), 8.46 (d, J=2.1 Hz, 1H), 8.67 (dd, J=6.0 Hz, J=1.8 Hz, 1H), 8.84 (d, J=2.1 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05629325
Source datasetuspto-grants-1997_05
ORD IDord-ced87e675ed7489c800811500c13562b
Source noteuspto-grants-1997_05