Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 635313Generated: October 29, 2026

HCID 178505853, compound → HCID 178505854, compound

https://huagongshe.com/reaction/635313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178505853HCID 178505853—
CatalystNickelHCID 935—
SolventEthanolHCID 702—
ProductHCID 178505854HCID 178505854—

Reaction Steps

5-Benzyl-3-(3-(4-(4-fluorophenyl)piperazin-1-yl)propyl)-4,5,6,7-tetrahydro-2H-pyrazolo[4,3-c]pyridine (0.5 g) obtained in Example 139 was dissolved in ethanol (10 ml), and Raney nickel (0.2 g) was added to perform catalytic reduction. After the completion of the reaction, the reaction mixture was filtered through celite and the filtrate was concentrated under reduced pressure. The obtained residue was subjected to silica gel column chromatography to give 3-(3-(4-(4-fluorophenyl)piperazin-1-yl)propyl)-4,5,6,7-tetrahydro-2H-pyrazolo[4,3-c]pyridine,

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06187774B1
Source datasetuspto-grants-2001_02
ORD IDord-4c44d1b485b34f7ba5034e4af75bc986
Source noteuspto-grants-2001_02