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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 219703Generated: October 27, 2026

Triethylamine → Acetic acid 3-[4-(2-tert-butyl-6-cyclobutyl-pyrimidin-4-yl)-piperazin-1-yl]-propyl ester

https://huagongshe.com/reaction/219703

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Propanol, 3-chloro-, acetateHCID 12334—
Reactant2-tert-Butyl-4-cyclobutyl-6-(piperazin-1-yl)pyrimidineHCID 66673390—
SolventDimethylformamideHCID 6228—
ProductAcetic acid 3-[4-(2-tert-butyl-6-cyclobutyl-pyrimidin-4-yl)-piperazin-1-yl]-propyl esterHCID 69025431—

Reaction Conditions

Temperature80 °C

Reaction Steps

5.5 g of 2-tert-butyl-4-piperazin-1-yl-6-cyclobutyl-pyrimidine (20.0 mmol), 3.15 g of acetic acid 3-chloro-propyl ester (23.1 mmol) and 2.76 g of triethylamine (27.3 mmol) were dissolved in 70 ml of dimethylformamide and stirred for 12 h at 80° C. After cooling, the dimethylformamide was evaporated, and the reaction mixture was partitioned between water and ethyl acetate. The organic layer was dried over magnesium sulfate, filtered, and the solvent was evaporated. The crude product (7 g) was directly used in the subsequent reaction step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202868B2
Source datasetuspto-grants-2012_06
ORD IDord-9f63be50d3af44f18c736260120ee1a6
Source noteuspto-grants-2012_06