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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1369543Generated: November 3, 2026

1-Methylpiperazine → HCID 22291120, compound

https://huagongshe.com/reaction/1369543

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
ReactantHCID 22291075HCID 22291075—
ProductHCID 22291120HCID 22291120—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of N-methylpiperazine (3 ml) and N-(5-{3-[N-(2-methoxyethyl)-N-methylamino]benzamido}-2-methylphenyl)-3-chloromethylbenzamide (0.21 g) was stirred and heated to 80° C. for 3 hours. The mixture was cooled to ambient temperature and partitioned between ethyl acetate and water. The organic phase was evaporated and the residue was triturated under diethyl ether. There was thus obtained the title compound (0.17 g); NMR Spectrum: (DMSOd6) 2.17 (d, 6H), 2.33 (m, 8H), 2.98 (s, 3H), 3.23 (s, 3H), 3.50 (m, 6H), 6.87 (d, 1H), 7.2 (m, 4H), 7.46 (m, 2H), 7.57 (m, 1H), 7.8 (s, 1H), 7.86 (m, 2H), 9.87 (s, 1H), 10.06 (s, 1H); Mass Spectrum: M+H+ 530.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06579872B1
Source datasetuspto-grants-2003_06
ORD IDord-95bd7a7be1764bca93da2fdf65313dc4
Source noteuspto-grants-2003_06