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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850333Generated: October 30, 2026

1-(4-{3-[1-(1H-Benzoimidazole-2-carbonyl)-azetidin-3-YL]-pyrazin-2-YL}-3,6-dihydro-2H-pyridin-1-YL)-ethanone → 1-(4-{3-[1-(1H-benzoimidazole-2-carbonyl)-azetidin-3-yl]-pyrazin-2-yl}-piperidin-1-yl)-ethanone

https://huagongshe.com/reaction/1850333

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-{3-[1-(1H-Benzoimidazole-2-carbonyl)-azetidin-3-YL]-pyrazin-2-YL}-3,6-dihydro-2H-pyridin-1-YL)-ethanoneHCID 58546855—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product1-(4-{3-[1-(1H-benzoimidazole-2-carbonyl)-azetidin-3-yl]-pyrazin-2-yl}-piperidin-1-yl)-ethanoneHCID 5854682460%

Reaction Steps

A mixture of 1-(4-{3-[1-(1H-benzoimidazole-2-carbonyl)-azetidin-3-yl]-pyrazin-2-yl}-3,6-dihydro-2H-pyridin-1-yl)-ethanone (170 mg, 0.42 mmol) and wet Pd—C (50%, 50 mg) in MeOH (30 mL) was stirred under H2 (30 psi) at RT for 2 h then the reaction mixture was filtered through CELITE® and washed with MeOH. The filtrate was concentrated in vacuo and the residue was purified by ISCO silica gel column (10% to 50% EtOAc in petroleum ether) to give 1-(4-{3-[1-(1H-benzoimidazole-2-carbonyl)-azetidin-3-yl]-pyrazin-2-yl}-piperidin-1-yl)-ethanone (101 mg, 0.25 mmol, 60% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957073B2
Source datasetuspto-grants-2015_02
ORD IDord-2e91afb5e4b24ce2aa47b0fdfb2da7ec
Source noteuspto-grants-2015_02