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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 603213Generated: October 29, 2026

Phenyl isocyanate → tert-Butyl (3S)-3-{[4-(anilinocarbonyl)piperazin-1-yl]methyl}piperidine-1-carboxylate

https://huagongshe.com/reaction/603213

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyl isocyanateHCID 7672—
Reactanttert-butyl (3S)-3-(piperazin-1-ylmethyl)piperidine-1-carboxylateHCID 24886660—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
Producttert-Butyl (3S)-3-{[4-(anilinocarbonyl)piperazin-1-yl]methyl}piperidine-1-carboxylateHCID 5765678480.5%

Reaction Steps

tert-Butyl (3S)-3-(piperazin-1-ylmethyl)piperidine-1-carboxylate (3.5 g) and phenyl isocyanate (1.62 g) were stirred in toluene (50 ml) at room temperature for 20 h. The solvent was then concentrated in-vacuo to afford a white solid. The solid was dissolved in methanol and passed through an SCX2 column. The SCX2 column was then flushed with 5% ammonia in methanol solution. The solution was collected and the solvent removed under reduced pressure. The resultant solid was re-crystallised from EtOAc and isoHexane, to afford the desired product as a white solid (4 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07906645B2
Source datasetuspto-grants-2011_03
ORD IDord-96cc74bb4ac841f29741e3320a9951cf
Source noteuspto-grants-2011_03