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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2364748Generated: October 31, 2026

(2S)-N,N-dibenzyl-2-methoxy-3-(4-methylpiperazin-1-yl)propan-1-amine → (2S)-2-methoxy-3-(4-methylpiperazin-1-yl)propan-1-amine

https://huagongshe.com/reaction/2364748

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2S)-N,N-dibenzyl-2-methoxy-3-(4-methylpiperazin-1-yl)propan-1-amineHCID 68107005—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product(2S)-2-methoxy-3-(4-methylpiperazin-1-yl)propan-1-amineHCID 68107783—

Reaction Steps

(2S)—N,N-Dibenzyl-2-methoxy-3-(4-methylpiperazin-1-yl)propan-1-amine 38a (500 mg, 1.36 mmol) was dissolved in 20 mL of methanol followed by the addition of palladium/carbon (100 mg, 10%), filled with hydrogen for three times. The reaction mixture was stirred at room temperature for 12 hours and filtered. The filtrate was concentrated under reduced pressure to obtain the crude title compound (2S)-2-methoxy-3-(4-methylpiperazin-1-yl)propan-1-amine 38b (250 mg, as a yellow oil liquid), which was used in the next step without further furification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691822B2
Source datasetuspto-grants-2014_04
ORD IDord-f3d535d395404237adc83a6fa40fcdc9
Source noteuspto-grants-2014_04