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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 574253Generated: October 29, 2026

Piperazin-2-one → HCID 67142728, compound

https://huagongshe.com/reaction/574253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazin-2-oneHCID 231360—
Reactanttert-butyl N-[(1R)-2-[5-bromo-3-[(2,6-difluorophenyl)methyl]-4-methyl-2,6-dioxopyrimidin-1-yl]-1-phenylethyl]carbamateHCID 11432814—
SolventAcetonitrileHCID 6342—
ProductHCID 67142728HCID 6714272858%

Reaction Conditions

Temperature140 °C

Reaction Steps

{(R)-2-[5-bromo-3-(2,6-difluoro-benzyl)-4-methyl-2,6-dioxo-3,6-dihydro-2H-pyrimidin-1-yl]-1-phenyl-ethyl}-carbamic acid tert-butyl ester (100 mg, 0.182 mmol) and piperazine-2-one (187 mg, 1.82 mmol) were placed into a microwave flask along the wall of which 1 mL of acetonitrile was then added. The solution was stirred at 140° C. for 3 hrs while being irradiated with microwaves. After concentration in a vacuum, the concentrate was purified by column chromatography eluting with a dichloromethane/methanol (35/1) eluent to afford 60 mg of the compound as a yellowish solid (yield 58%). 1H NMR (300 MHz, CDCl3) δ 1.36 (9H, s), 2.43 (3H, s), 2.86 (1H, m), 3.27 (2H, m), 3.50 (1H, m), 3.74 (1H, m), 4.07 (2H, m), 4.27 (1H, m), 5.04 (1H, m), 5.29 (2H, dd), 5.68 (1H, m), 6.30 (1H, m), 6.90 (2H, t), 7.22-7.37 (6H, m)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09034850B2
Source datasetuspto-grants-2015_05
ORD IDord-51f97bd9e07c46ac835c8e79707aeaeb
Source noteuspto-grants-2015_05