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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 926494Generated: November 1, 2026

1-Methyl-1H-1,2,3-triazole → (2,6-Dimethyl-4-pyridinyl)(1-methyl-1H-1,2,3-triazol-5-yl)methanone

https://huagongshe.com/reaction/926494

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Methyl-1H-1,2,3-triazoleHCID 140119—
ReactantN-Methoxy-N,2,6-trimethylisonicotinamideHCID 18736278—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product(2,6-Dimethyl-4-pyridinyl)(1-methyl-1H-1,2,3-triazol-5-yl)methanoneHCID 107502509—

Reaction Steps

A solution of n-BuLi (3.8 mL, 9.5 mmol, 2.5 M solution in hexane) was added slowly to a solution of 1-methyl-1H-1,2,3-triazole (0.83 g, 10 mmol) in THF (48 mL) at −50° C. After addition, stirring was continued for an additional 30 minutes and N-methoxy-N,2,6-trimethylisonicotinamide (0.97 g, 5.0 mmol, Intermediate 29: step a) dissolved in THF (12 mL) was slowly added. An additional 2 mL of THF was used to complete the quantitative addition. The mixture was stirred at −50° C. for 5 minutes then warmed to room temperature and stirred overnight. The solution was quenched with saturated aqueous NH4Cl. H2O was added and layers were separated. The aqueous layer was extracted with EtOAc and the combined organic extracts washed with brine, dried over MgSO4, filtered and evaporated in vacuo. The crude product was purified using flash column chromatography (0 to 100% EtOAc/DCM) to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09284308B2
Source datasetuspto-grants-2016_03
ORD IDord-29d853f380bd48a8b16114eeff8270bc
Source noteuspto-grants-2016_03