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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1978408Generated: October 25, 2026

Triethylamine → Triethylamine hydrochloride

https://huagongshe.com/reaction/1978408

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant(S)-(2,3-Dihydrobenzo[b][1,4]dioxin-2-yl)methyl methanesulfonateHCID 11128529—
ReactantN-(piperidin-4-ylmethyl)-5-thia-1,8b-diazaacenaphthylene-4-carboxamide dihydrochlorideHCID 21993937—
SolventEthanolHCID 702—
ProductTriethylamine hydrochlorideHCID 11130—
Product(R)-N-[1-(1,4-benzodioxan-2-ylmethyl)piperidin-4-ylmethyl)-5-thia-1,8b-diazaacenaphthylene-4-carboxamideHCID 9804407—

Reaction Steps

A solution of the above crude (S)-2-methanesulfonyloxymethyl-1,4-benzodioxane, 1.05 g (2.71 mM) of N-(piperidin-4-ylmethyl)-5-thia-1,8b-diazaacenaphthylene-4-carboxamide dihydrochloride, and 1.20 ml (8.64 mM) of triethylamine in 30 ml of ethanol was refluxed for 3 days. The solvent was then distilled off under reduced pressure and the residue was purified by silica gel column chromatography (ethyl acetate to ethyl acetate-methanol=4/1 to 3/1) to provide the title compound and triethylamine hydrochloride as a mixture. This mixture was diluted with ethyl acetate and washed serially with aqueous solution of sodium hydrogen carbonate, water, and saturated aqueous solution of NaCl. The organic layer was dried over MgSO4 and the solvent was distilled off to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06235731B1
Source datasetuspto-grants-2001_05
ORD IDord-c467df2bb67546778ec33b7939480055
Source noteuspto-grants-2001_05