Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 365894Generated: October 25, 2026

Triethylamine → 3-(1-Boc-2-(s)-azetidinylmethoxy)-6-chloro-5-(trimethylsilylethynyl)pyridine

https://huagongshe.com/reaction/365894

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTrimethylsilylacetyleneHCID 66111—
Reactant3-(1-BOC-2-(S)-azetidinylmethoxy)-5-bromo-6-chloropyridineHCID 22872667—
CatalystHCID 178418397HCID 178418397—
CatalystHCID 178505377HCID 178505377—
SolventTolueneHCID 1140—
Product3-(1-Boc-2-(s)-azetidinylmethoxy)-6-chloro-5-(trimethylsilylethynyl)pyridineHCID 2296182775%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 3-(1-BOC-2-(S)-azetidinylmethoxy)-5-bromo-6-chloropyridine (1.0 g, 2.6 mmol) in toluene (20 mL) was added NEt3 (1 mL), copper (I) iodine (50 mg, 10%), tetrakis(triphenylphosphine)palladium (0) (305 mg, 10%) and (trimethylsilyl)acetylene (0.45 mL, 3.18 mmol). The reaction mixture was stirred and heated at 100° C. for 16 h. Solvent was evaporated and the residue was chromatographed (silica gel; hexane/EtoAc, 5:1 to 2:1) to afford an oil (770 mg, 74%): 1H NMR (CDCl3, 300 MHz) δ 1.42 (s, 9H), 2.20-2.40 (m, 2H), 3.80-3.92 (m, 2H), 4.10 (m, 1H), 4.30 (m, 1H), 4.50 (m, 1H), 7.37 (d, 1H, J=3.0 Hz), 8.05 (d, 1H, J=3.0 Hz); MS (CI/NH3) m/z 395 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06127386
Source datasetuspto-grants-2000_10
ORD IDord-612e7439e0e449bba3d5cef409ba9ff5
Source noteuspto-grants-2000_10