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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1815641Generated: October 29, 2026

Piperidine → HCID 66929718, compound

https://huagongshe.com/reaction/1815641

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantHCID 66930031HCID 66930031—
SolventDimethylformamideHCID 6228—
ProductHCID 66929718HCID 66929718—

Reaction Conditions

Temperature25 °C

Reaction Steps

To tert-butyl 4-((1S)-1-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-2-hydroxyethyl)piperdine-1-carboxylate (0.95 g, 2.03 mmol) was added 20% piperidine in dimethylformamide (20 mL) all at once. The reaction was stirred overnight at 25° C. The dimethylformamide was evaporated off and the crude residue was subjected to flash chromatography using methylene chloride-methanol-ammonium hydroxide, 95-5-0.1% as eluent. This yielded the amine product as an oil that crystallized upon standing (0.392 g, 80%). MS (+ESI) 245.2 ([M+M]+); 189.2; 150.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06878742B2
Source datasetuspto-grants-2005_04
ORD IDord-3e190c9e800c4e888c89d19119d94ab7
Source noteuspto-grants-2005_04