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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 361813Generated: October 24, 2026

U 99363 → 4-[N-Methyl-N-(3-ethoxy-2-pyridinyl)amino]piperidine

https://huagongshe.com/en/reaction/361813

Reaction equation

Participants

RoleNameHCIDCharge
ReactantU 99363HCID 133107—
ReactantAmmonium formateHCID 2723923—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product4-[N-Methyl-N-(3-ethoxy-2-pyridinyl)amino]piperidineHCID 10847368—

Reaction Steps

A mixture of 1-benzyl-4-[N-methyl-N-(3-ethoxy-2-pyridinyl)amino]piperidine (EXAMPLE 70, 1.40 g), palladium-on-carbon (10%, 1.4 g) and ammonium formate (813 mg) in methanol (25 ml) is degassed, stirred at 65° for 45 min, cooled to 20°-25°, and filtered to remove catalyst. The filtrate is concentrated under reduced pressure to give the title compound, NMR (CDCl3) 7.83, 6.97, 6.71, 4.02, 3.88, 3.15, 2.88, 2.63, 1.75 and 1.46δ.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05866589
Source datasetuspto-grants-1999_02
ORD IDord-4794e628ec764be1bb45fce4998378a0
Source noteuspto-grants-1999_02