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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2171668Generated: November 1, 2026

HCID 86686203, compound → HCID 86686228, compound

https://huagongshe.com/reaction/2171668

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86686203HCID 86686203—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
ProductHCID 86686228HCID 8668622892.5%

Reaction Steps

1′-[3-({[tert-Butyl(dimethyl)silyl]oxy}methyl)-2-fluorophenyl]-1′,2′,3′,6′-tetrahydro-3,4′-bipyridine (257 mg) was mixed with EtOH (5 ml), and 10% palladium carbon (55 mg) was added thereto under argon atmosphere, followed by stirring at room temperature overnight under hydrogen atmosphere. The reaction mixture was filtered using Celite as a filtration adjuvant, and the filtrate was concentrated under reduced pressure to obtain 3-{1-[3-({[tert-butyl(dimethyl)silyl]oxy}methyl)-2-fluorophenyl]piperidin-4-yl}pyridine (239 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051283B2
Source datasetuspto-grants-2015_06
ORD IDord-5825a4fa6e5a4bfaba061a5d4af7be95
Source noteuspto-grants-2015_06