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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704589Generated: October 29, 2026

Triethylamine → 1-(1,4-Dioxaspiro[4,5]dec-8-ylacetyl)-4-(2-pyridinyl)piperazine

https://huagongshe.com/reaction/704589

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantIsobutyl chloroformateHCID 62365—
Reactant1-(2-Pyridyl)piperazineHCID 94459—
Reactant2-(1,4-Dioxaspiro(4.5)decan-8-yl)acetic acidHCID 15101121—
SolventDichloromethaneHCID 6344—
Product1-(1,4-Dioxaspiro[4,5]dec-8-ylacetyl)-4-(2-pyridinyl)piperazineHCID 1510112273.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

An ice-cold solution of 1,4-dioxaspiro[4,5]-decane-8-acetic acid (20.0 g) (Example G) and triethylamine (20.9 ml) in 100 ml of dichloromethane is treated dropwise with a solution of isobutyl chloroformate (19.4 ml) in 100 ml of dichloromethane under nitrogen. The resulting solution is stirred at 0° C. for 10 minutes and a solution of 1-(2-pyridyl)-piperazine (32.59 g) in 100 ml of dichloromethane is added dropwise. The mixture is stirred at 0° C. for 15 minutes and then at room temperature for one hour. After washing with 1 L of a saturated solution of sodium bicarbonate, the organic phase is dried over magnesium sulfate and concentrated in vacuo. The crude product is purified by MPLC (silica; ethyl acetate) to give 25.50 g of the title compound as a colorless solid; mp 113°-116° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04988699
Source datasetuspto-grants-1991_01
ORD IDord-f855816bccda45eb85e77de550946b54
Source noteuspto-grants-1991_01