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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2375839Generated: October 29, 2026

1-Methylpiperazine → Phenylmethyl α,α,4-trimethyl-1-piperazinepropanoate

https://huagongshe.com/reaction/2375839

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
ReactantHCID 58710084HCID 58710084—
ProductPhenylmethyl α,α,4-trimethyl-1-piperazinepropanoateHCID 58710079—

Reaction Steps

The procedure for benzyl-2,2-dimethyl-3-piperidin-1-ylpropanoate was followed except for replacing piperidine with 1-methylpiperazine. Purification via silica gel chromatography (5% EtOAc in hexane) afforded the title compound as a yellow oil. MS (ES+): m/z: 291.20 (100) [MH+]. HPLC: tr=2.08 min (ZQ2000: polar—5 min). 1H NMR (400 MHz, CDCl3): δ=1.18 (s, 6H), 2.09 (s, 3H), 2.23-2.33 (m, 4H), 2.39-2.50 (m, 6H), 5.11 (s, 2H) 7.31-7.36 (m, 5H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07465726B2
Source datasetuspto-grants-2008_12
ORD IDord-939050c4fad34c24848925d0c6915201
Source noteuspto-grants-2008_12