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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzidobenzeneHCID 69319—
ReactantDiisopropylethylamineHCID 81531—
Reactant1-Propargyl-3-methoxypyridine-2-oneHCID 71655522—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product1-Phenyltriazolylmethyl-3-methoxypyridine-2-oneHCID 17848764292%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871728B2
Source datasetuspto-grants-2014_10
ORD IDord-9bf95ba9cb8a4f1ca877deefdf743549
Source noteuspto-grants-2014_10