Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2238683Generated: October 31, 2026

HCID 131728130, compound → HCID 131728131, compound

https://huagongshe.com/reaction/2238683

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 131728130HCID 131728130—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
SolventTetrahydrofuranHCID 8028—
ProductHCID 131728131HCID 131728131106.1%

Reaction Steps

50 mg of the t-butyl((1S)-1-{4-[1-(trifluoroacetyl)-1,2,3,6-tetrahydropyridin-4-yl]phenyl}ethyl)carbamate [154-3] was dissolved in 3 mL of tetrahydrofuran, then a catalytic amount of 10% palladiumcarbon catalyst was added thereto, and stirred at room temperature for 1 hour in a hydrogen atmosphere. The insolubles were filtered through celite, the filtrate was concentrated under reduced pressure, and 53.3 mg of t-butyl((1S)-1-{4-[1-(trifluoroacetyl)piperidin-4-yl]phenyl}ethyl)carbamate [155-1] was obtained as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07718801B2
Source datasetuspto-grants-2010_05
ORD IDord-930805f185cf441c9c0674cbea6c542a
Source noteuspto-grants-2010_05