Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2368109Generated: November 3, 2026

HCID 67447624, compound → HCID 86658703, compound

https://huagongshe.com/reaction/2368109

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67447624HCID 67447624—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
ProductHCID 86658703HCID 86658703—

Reaction Steps

To a solution of benzyl 4-{(3S)-3-[(tert-butoxycarbonyl)amino]butyl}piperazine-1-carboxylate (1.10 g) in ethanol (10 mL) was added 10% palladium carbon (1.50 g), and the mixture was stirred at room temperature for 30 min under a hydrogen atmosphere. The reaction mixture was filtered, and the filtrate was evaporated under reduced pressure to give tert-butyl [(1S)-1-methyl-3-(piperazin-1-yl)propyl]carbamate. By a method similar to Example 1, steps F to H, and using the obtained compound, the title compound was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08703758B2
Source datasetuspto-grants-2014_04
ORD IDord-736b5277df89418780373ce38d50d8b8
Source noteuspto-grants-2014_04