HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 539525Generated: October 26, 2026
Azidobenzene → 1-Phenyltriazolylmethyl-3-methoxypyridine-2-one
https://huagongshe.com/reaction/539525
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azidobenzene | HCID 69319 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-Propargyl-3-methoxypyridine-2-one | HCID 71655522 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Phenyltriazolylmethyl-3-methoxypyridine-2-one | HCID 178487642 | 92% |
Reaction Steps
150 (0.32 g, 1.951 mmol) and phenylazide (0.348 g, 2.926 mmol) were dissolved in anhydrous THF (10 mL) and stirred under argon at room temperature. Copper (I) iodide (0.011 g, 0.07 mmol) and Hunig's base (0.1 mL) were then added to the reaction mixture, and stirring continued for 4 h. The reaction mixture was diluted with CH2Cl2 (40 mL) and washed with 1:4 NH4OH/saturated NH4Cl (3×30 mL) and saturated NH4Cl (30 mL). The organic layer was dried over Na2SO4 and concentrated in vacuo. The crude product was triturated with hexanes to give 510 mg (92%) of white solid 151a. 1H NMR (CDCl3, 400 MHz) δ 3.58 (3H, s), 5.11 (2H, s), 5.93 (1H, t, J=7.6), 6.42 (1H, d, J=7.2), 7.07 (1H, d, J=6.4), 7.16-7.20 (1H, m), 7.26 (2H, t, J=7.6), 7.49 (2H, d, J=8.0); 13C NMR (CDCl3, 100 MHz) δ 44.2, 55.2, 104.7, 112.0, 119.7, 121.8, 127.9, 128.1, 129.0, 136.2, 142.8, 149.3, 157.2. HRMS (EI) calcd for C15H14N4O2 [M]+ 282.1117. found 282.1115.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08871728B2 |
|---|
| Source dataset | uspto-grants-2014_10 |
|---|
| ORD ID | ord-9bf95ba9cb8a4f1ca877deefdf743549 |
|---|
| Source note | uspto-grants-2014_10 |
|---|