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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 365897Generated: October 25, 2026

Allyltributylstannane → 5-Allyl-3-(1-boc-2-(s)-azetidinylmethoxy)-6-chloropyridine

https://huagongshe.com/reaction/365897

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyltributylstannaneHCID 90628—
Reactant3-(1-BOC-2-(S)-azetidinylmethoxy)-5-bromo-6-chloropyridineHCID 22872667—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventTolueneHCID 1140—
Product5-Allyl-3-(1-boc-2-(s)-azetidinylmethoxy)-6-chloropyridineHCID 2296188483.5%

Reaction Steps

3-(1-BOC-2-(S)-Azetidinylmethoxy)-5-bromo-6-chloropyridine (1.0 g, 2.65 mmol) in toluene (10 mL) was added tetrakis(triphenylphosphine) palladium (100 mg) and allyltributyltin (0.99 mL, 3.18 mmol). The mixture was stirred and refluxed for two days. Solvent was evaporated and the residue was chromatographed (silica gel; hexane/EtOAc, 5:1 to 1:1) to afford an oil (750 mg, 83%): 1H NMR (CDCl3, 300 MHz) δ 1.42 (s, 9H), 2.20-2.40 (m, 2H), 3.43 (d, 2H, J=6.5 Hz), 3.88 (t, 2H, J=7.0 Hz), 4.12 (m, 1H), 4.30 (m, 1H), 4.50 (m, 1H), 5.10-5.20 (m, 2H), 5.92 (m, 1H), 7.18 (d, J=3.0 Hz), 7.98 (d, 1H, J=3.0 Hz); MS (CI/NH3) m/z 339 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06127386
Source datasetuspto-grants-2000_10
ORD IDord-c70821849c5f4f129513a8fe4fd6e576
Source noteuspto-grants-2000_10