Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828207Generated: October 31, 2026

HCID 69585305, compound → HCID 69585305, compound

https://huagongshe.com/reaction/1828207

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 69585305HCID 69585305—
CatalystAcetic AcidHCID 176—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 69585305HCID 69585305—
ProductHCID 69585537HCID 69585537—

Reaction Steps

5-[2-(1-Benzyl-piperidin-4-yl)-3-m-tolyl-1H-pyrazol-4-yl]-1,3-diethyl-1,3-dihydro-benzoimidazol-2-one is prepared according to the procedures described in Example 334. 5-[2-(1-Benzyl-piperidin-4-yl)-3-m-tolyl-1H-pyrazol-4-yl]-1,3-diethyl-1,3-dihydro-benzoimidazol-2-one (180 mg) is diluted with ethanol (5 mL) and acetic acid (5 drops). The mixture is then treated with 5% Pd/C and shaken under an atmosphere of hydrogen for 8 hours. The mixture is then filtered and concentrated to give 1,3-Diethyl-5-(2-piperidin-4-yl-3-m-tolyl-1H-pyrazol-4-yl)-1,3-dihydro-benzoimidazol-2-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07056918B2
Source datasetuspto-grants-2006_06
ORD IDord-8958de52393244d2887a7df73ce1f1a4
Source noteuspto-grants-2006_06