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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1712285Generated: November 1, 2026

1,2,4-Triazolylsodium → tert-Butyl 4-{4-[3-(2-methoxybenzyloxy)propoxy]phenyl}-3-{2-[2-(2-[1,2,4]triazol-1-ylethyl)phenoxy]ethoxy}piperidine-1-carboxylate

https://huagongshe.com/reaction/1712285

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2,4-TriazolylsodiumHCID 54719965—
ReactantTert-butyl 4-{4-[3-(2-methoxybenzyloxy)propoxy]phenyl}-3-(2-{2-[2-(toluene-4-sulphonyloxy)ethyl]phenoxy}-ethoxy)piperidine-1-carboxylateHCID 86609986—
SolventDimethylformamideHCID 6228—
Solventtert-Butyl methyl etherHCID 15413—
Producttert-Butyl 4-{4-[3-(2-methoxybenzyloxy)propoxy]phenyl}-3-{2-[2-(2-[1,2,4]triazol-1-ylethyl)phenoxy]ethoxy}piperidine-1-carboxylateHCID 68497847—

Reaction Conditions

Temperature90 °C

Reaction Steps

0.051 g of sodium 1,2,4-triazolide is admixed with a solution of 0.10 g of tert-butyl 4-{4-[3-(2-methoxybenzyloxy)propoxy]phenyl}-3-(2-{2-[2-(toluene-4-sulphonyloxy)ethyl]phenoxy}-ethoxy)piperidine-1-carboxylate in 3 ml of N,N-dimethylformamide. The reaction mixture is stirred at 90° C. over 40 minutes. The mixture is cooled to room temperature, diluted with tert-butyl methyl ether and washed with water. The water phase is extracted with tert-butyl methyl ether. The combined organic phases are dried over sodium sulphate and concentrated by evaporation. The title compound is obtained as a colourless oil from the residue by means of flash chromatography (SiO2 60F). Rf=0.13 (2:1 EtOAc-heptane); Rt=5.66.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790715B2
Source datasetuspto-grants-2010_09
ORD IDord-8201767236424c5db3e6e1d6d80364ce
Source noteuspto-grants-2010_09