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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 365874Generated: October 30, 2026

Sodium Carbonate → 3-(1-Boc-2-(s)-azetidinylmethoxy)-5-(2-thienyl)pyridine

https://huagongshe.com/reaction/365874

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2-Thiopheneboronic acidHCID 2733960—
Reactant(S)-Tert-butyl 2-(((5-bromopyridin-3-YL)oxy)methyl)azetidine-1-carboxylateHCID 10688713—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
Product3-(1-Boc-2-(s)-azetidinylmethoxy)-5-(2-thienyl)pyridineHCID 2296181557.7%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a mixture of 3-(1-BOC-2-(S)-azetidinylmethoxy)-5-bromopyridine (0.42 g, 1.2 mmol), tetrakis(triphenylphosphine)palladium(0) (40 mg, 0.034 mmol), sodium carbonate (2.0 M, 2 mL) in toluene (10 mL) was added 2-thienylboronic acid (0.38 g, 3.0 mmol). The reaction mixture was stirred and heated at 80° C. for 16 h. Solvent was evaporated. The residue was chromatographed (silica gel; hexane/EtOAC, 10:1 to 2:1) to afford an oil (0.24 g, 57%): 1H NMR (CDCl3, 300 MHz) δ1.42 (s, 9H), 2.26-2.90 (m, 2H), 3.86-3.94 (m, 2H), 4.20 (m, 1H), 4.39 (m, 1H), 4.55 (m, 1H), 7.12 (m, 1H), 7.36 (s, 1H), 7.44 (s, 1H), 8.26 (s, 1H), 8.50 (s, 1H); MS (CI/NH3) m/z 347 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06127386
Source datasetuspto-grants-2000_10
ORD IDord-ec0839a3f68b49f19833a3ed87daf309
Source noteuspto-grants-2000_10