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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2227844Generated: November 1, 2026

Piperazine → (R)-1-(4-Piperazin-1-yl-pyrimidin-2-yl)-ethyl acetate

https://huagongshe.com/reaction/2227844

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
Reactant(R)-1-(4-methanesulfonyloxy-pyrimidin-2-yl)-ethyl acetateHCID 54125954—
SolventTetrahydrofuranHCID 8028—
Product(R)-1-(4-Piperazin-1-yl-pyrimidin-2-yl)-ethyl acetateHCID 1092295088%

Reaction Steps

A mixture of (R)-1-(4-methanesulfonyloxy-pyrimidin-2-yl)-ethyl acetate (prepared according to the method of Preparation Six, 24.1 g, 92 mmol) and piperazine (16.0 g, 184 mmol) in tetrahydrofuran (200 mL) was heated at reflux for 1 h. This mixture was cooled, filtered, concentrated, and purified by flash column chromatography (9:1 dichloromethane/methanol) to give 24.4 g (88%) of the title compound as an oil. 1H NMR (CDCl3, 300 MHz) δ1.56 (d, 3H), 2.25 (s, 3H), 2.83 (m, 4H), 3.63 (m, 4H), 5.54 (q, 1H), 6.38 (d, 1H), 8.24 (d, 1H); MS (CI) 251 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06414149B1
Source datasetuspto-grants-2002_07
ORD IDord-b9f7f1921bbb48e98a81873f448550ac
Source noteuspto-grants-2002_07