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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 225435Generated: October 30, 2026

1-Methylpiperazine → HCID 178428247, compound

https://huagongshe.com/reaction/225435

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-6, 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 numberUS07557106B2
Source datasetuspto-grants-2009_07
ORD IDord-7d47b094840b4240855b42d02bc5bb85
Source noteuspto-grants-2009_07