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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 70201Generated: October 28, 2026

Ammonium formate → Tert-butyl 2-((pyridin-3-yloxy)methyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/70201

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
Reactant1-Tert-butyl 4-benzyl 2-((pyridin-3-yloxy)methyl)piperazine-1,4-dicarboxylateHCID 59671606—
CatalystPalladium hydroxideHCID 9942167—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
ProductTert-butyl 2-((pyridin-3-yloxy)methyl)piperazine-1-carboxylateHCID 5967147387.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

Palladium hydroxide on carbon (˜40% palladium, 0.170 g, 0.12 mmol) was added to a solution of 1-tert-butyl 4-benzyl 2-((pyridin-3-yloxy)methyl)piperazine-1,4-dicarboxylate (0.649 g, 1.52 mmol) and ammonium formate (0.191 g, 3.03 mmol) in EtOH (10 mL), and the reaction mixture was heated to 80° C. for 2 h. Upon cooling to rt, the reaction mixture was diluted with EtOAc (40 mL) and washed with water (3×30 mL) and brine (30 mL). The organics were dried over Na2SO4, filtered, and concentrated under reduced pressure, yielding 388.4 mg (87%) of the desired product as a white, waxy solid. LC-MS: RT=3.90 min, [M+H]+=294.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822472B2
Source datasetuspto-grants-2014_09
ORD IDord-68f5d6a81e6b46de9ec8733c8f0b32b4
Source noteuspto-grants-2014_09