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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 924597Generated: November 2, 2026

Hydrochloric Acid → 5-Methoxy-[1,2,5]triazepane hydrochloride salt

https://huagongshe.com/reaction/924597

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,4-DioxaneHCID 31275—
Reactant5-Methoxy-[1,2,5]triazepane-1,2-dicarboxylic acid di-tert-butyl ester hydrochloride saltHCID 86719911—
SolventEthyl AcetateHCID 8857—
Product5-Methoxy-[1,2,5]triazepane hydrochloride saltHCID 86719913—

Reaction Conditions

Temperature90 °C

Reaction Steps

A solution of 5-methoxy-[1,2,5]triazepane-1,2-dicarboxylic acid di-tert-butyl ester in diethyl ether was treated with gaseous hydrogen chloride to generate a white precipitate. The solid was filtered, washed with diethyl ether and dried to afford 5-methoxy-[1,2,5]triazepane-1,2-dicarboxylic acid di-tert-butyl ester hydrochloride salt. To a suspension of 5-methoxy-[1,2,5]triazepane-1,2-dicarboxylic acid di-tert-butyl ester hydrochloride salt (2.5 g, 6.8 mmol) in ethyl acetate (10 ml) was added a solution of hydrogen chloride in 1,4-dioxane (4 M, 9 ml, 36.0 mmol) at room temperature dropwise. The reaction mixture was heated at 90° C. for one hour, the solvent evaporated, the residue washed with diethyl ether and dried in vacuo. Yield: 1.4 g of 5-methoxy-[1,2,5]triazepane hydrochloride salt (compound P4.2) as a yellowish solid, this material was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09282743B2
Source datasetuspto-grants-2016_03
ORD IDord-8c9e8fabc04f4d9ea187ee32a5cdca92
Source noteuspto-grants-2016_03