Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444100Generated: November 2, 2026

1,4-Dioxane hydrochloride → Ethyl 5-chloro-6-(piperazin-1-YL)nicotinate

https://huagongshe.com/reaction/1444100

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-Dioxane hydrochlorideHCID 20443148—
ReactantEthyl 6-[1-(tert-butoxycarbonyl)piperazin-4-yl]-5-chloronicotinateHCID 59168365—
Solvent1,4-DioxaneHCID 31275—
ProductEthyl 5-chloro-6-(piperazin-1-YL)nicotinateHCID 22028944—

Reaction Conditions

Temperature50 °C

Reaction Steps

Dissolve a solution of 4-(3-chloro-5-ethoxycarbonyl-pyridin-2-yl)piperazine-1-carboxylic acid tert-butyl ester (7.78 g, 0.021 mol) in dioxane, and then add a solution of 4M HCl/dioxane (12 mL). Stir at 50° C. for 2 h, and then add additional 4M HCl/dioxane (5 mL) and stir for an additional 1 h. Cool the mixture in ice, collect the precipitate and wash with ether. Prepare the freebase by partitioning between EtOAc and 10% NaOH solution. Dry the organic layer (Na2SO4) and concentrate under reduced pressure to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662830B2
Source datasetuspto-grants-2010_02
ORD IDord-dfb29871171e443c921a6204d3e55efd
Source noteuspto-grants-2010_02