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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2386294Generated: October 31, 2026

1-Methylpiperazine → HCID 178428247, compound

https://huagongshe.com/reaction/2386294

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
ReactantHCID 178428223HCID 178428223—
ProductHCID 178428247HCID 178428247—

Reaction Steps

Compound D (2.373 g, 5.92 mmol) was treated with N-methylpiperazine (10 ml) and the mixture stirred at 110° for 2 hours. The excess N-methylpiperazine was removed in vacuo then the residue was dissolved in ethyl acetate, washed with aqueous sodium bicarbonate solution, dried over magnesium sulphate, and concentrated. The residue was crystallised from methanol to give colourless crystals of desired product V-1 (1.82 g, 66%), 1H-NMR DMSO-d6, δ 0.81 (4H, d), 1.79 (1H, m), 2.01 (3H, s), 2.18 (3H, s), 2.30 (4H, m), 3.35 (masked signal), 5.42 (1H, s), 6.02 (1H, br s), 7.47 (2H, d), 7.69 (2H, d), 9.22 (1H, s), 10.39 (1H, s), 11.69 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08268829B2
Source datasetuspto-grants-2012_09
ORD IDord-d69d024b65fe43749603834a6c5d3ee0
Source noteuspto-grants-2012_09