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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402366Generated: November 1, 2026

Water → Methyl 6-((4-(2-fluorophenyl)-1-methyl-1H-1,2,3-triazol-5-yl)methoxy)nicotinate

https://huagongshe.com/reaction/402366

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
ReactantMethyl 6-chloropyridine-3-carboxylateHCID 254249—
Reactant(4-(2-Fluorophenyl)-1-methyl-1H-1,2,3-triazol-5-yl)methanolHCID 67498210—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 6-((4-(2-fluorophenyl)-1-methyl-1H-1,2,3-triazol-5-yl)methoxy)nicotinateHCID 5733449467%

Reaction Steps

A solution of (4-(2-fluorophenyl)-1-methyl-1H-1,2,3-triazol-5-yl)methanol (100 mg, 0.48 mmol) in THF (1.4 mL) was added dropwise at 0° C. to a suspension of NaH (60% in oil, 21 mg, 0.53 mmol) in THF (0.7 mL) and the reaction mixture was then stirred at room temperature for 30 min. Then a solution of methyl 6-chloronicotinate (91 mg, 0.53 mmol) in THF (1 mL) was added dropwise at 0° C. and the reaction mixture stirred at room temperature for 16 h. The mixture was then poured into water extracted with ethyl acetate and the combined organic extracts washed with brine, dried over sodium sulphate, filtered and evaporated. Purification by chromatography (silica, 0 to 100% ethyl acetate in heptane) afforded the title compound (110 mg, 67%) as a colourless gum. MS: m/e=343.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08742097B2
Source datasetuspto-grants-2014_06
ORD IDord-8c1cac9016774b5ab46638452efde75b
Source noteuspto-grants-2014_06