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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 708327Generated: October 30, 2026

1-Methylpiperazine → 2-(4-methylpiperazin-1-yl)-N-(prop-2-yn-1-yl)acetamide

https://huagongshe.com/reaction/708327

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
Reactant2-bromo-N-(prop-2-yn-1-yl)acetamideHCID 11159617—
SolventDichloromethaneHCID 6344—
Product2-(4-methylpiperazin-1-yl)-N-(prop-2-yn-1-yl)acetamideHCID 7891250849%

Reaction Steps

To a solution of 2-bromo-N-(prop-2-yn-1-yl)acetamide (0.7 g, 3.98 mmol) in DCM (10 mL) added N-methyl piperazine (0.66 mL, 5.96 mmol) drop wise. Reaction mixture stirred at rt for 16 h, diluted with DCM and washed with water and brine. The organic layer was dried over Na2SO4 and concentrated in vacuo. The crude residue was triturated with ether-pentane, affording the title compound (0.38 g, 49%); LCMS: m/z=196.15 (M+1); 1H NMR (300 MHz, DMSO-d6) δ 8.06 (d, J=6.1 Hz, 1H), 3.86 (dd, J=5.9, 2.5 Hz, 2H), 3.07 (t, J=2.5 Hz, 1H), 2.91 (s, 2H), 2.47-2.25 (m, 8H), 2.15 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174978B2
Source datasetuspto-grants-2015_11
ORD IDord-885730bb68a144cb991ec2be0bb66ebd
Source noteuspto-grants-2015_11