Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2364709Generated: October 30, 2026

benzyl N-[(2R)-2-hydroxy-3-(4-methylpiperazin-1-yl)propyl]carbamate → (2R)-1-amino-3-(4-methylpiperazin-1-yl)propan-2-ol

https://huagongshe.com/reaction/2364709

Reaction equation

Participants

RoleNameHCIDCharge
Reactantbenzyl N-[(2R)-2-hydroxy-3-(4-methylpiperazin-1-yl)propyl]carbamateHCID 68108054—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product(2R)-1-amino-3-(4-methylpiperazin-1-yl)propan-2-olHCID 28279114106.9%

Reaction Steps

Benzyl N-[(2R)-2-hydroxy-3-(4-methylpiperazin-1-yl)propyl]carbamate 20d (830 mg, 2.70 mmol) was dissolved in 40 mL of methanol followed by the addition of palladium/carbon (85 mg, 10%), filled with hydrogen three times. The reaction solution was stirred for 12 hours and filtered. The filtrate was concentrated under reduced pressure to obtain the crude title compound (2R)-1-amino-3-(4-methylpiperazin-1-yl)propan-2-ol 20e (500 mg) as a light yellow oil, 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-cca94c7489ee499f94888eb3960ca14b
Source noteuspto-grants-2014_04