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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 558177Generated: October 31, 2026

tert-butyl N-[(3S)-piperidin-3-yl]carbamate → 4-(N-Boc-amino)piperidine

https://huagongshe.com/reaction/558177

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl N-[(3S)-piperidin-3-yl]carbamateHCID 1514171—
Reactant(3S)-(-)-3-(tert-Butoxycarbonylamino)pyrrolidineHCID 1514396—
Product4-(N-Boc-amino)piperidineHCID 723833—

Reaction Steps

3-(S)-tert-butoxycarbonylaminopiperidine (B=formula (2)) and 3-(S)-tert-butoxycarbonylaminopyrrolidine (B=formula (3)) (Synth. Comm. 1998, 28, 3919) in the last two cases Y═COOC(CH3)3; tert-butyl 8-azabicyclo[3.2.1]-oct-3-yl-exo-carbamate (B=formula (4), tert-butyl 8-azabicyclo[3.2.1]-oct-3-yl-endo-carbamate (B=formula (5)) (J. Med. Chem. 1991, 34, 656), tert-butyl 9-azabicyclo[3.3.1]-non-3-yl exo-carbamate (B=formula (6)) and tert-butyl 9-azabicyclo-[3.3.1]-non-3-yl-endo-carbamate (B=formula (7)), (J. Med. Chem. 1993, 36, 3720)) (Y═COOC(CH3)3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063045B2
Source datasetuspto-grants-2011_11
ORD IDord-acec90d3ff34433392593714364ab2d1
Source noteuspto-grants-2011_11