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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Trimethylsilylacetylene | HCID 66111 | — |
| Reactant | 3-(1-BOC-2-(S)-azetidinylmethoxy)-5-bromo-6-chloropyridine | HCID 22872667 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Catalyst | HCID 178505377 | HCID 178505377 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-(1-Boc-2-(s)-azetidinylmethoxy)-6-chloro-5-(trimethylsilylethynyl)pyridine | HCID 22961827 | 75% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06127386 |
|---|
| Source dataset | uspto-grants-2000_10 |
|---|
| ORD ID | ord-612e7439e0e449bba3d5cef409ba9ff5 |
|---|
| Source note | uspto-grants-2000_10 |
|---|