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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473708Generated: October 30, 2026

tert-butyl 4-(3-(4-(pyridin-2-ylamino)phenoxy)pyrazin-2-yl)-5,6-dihydropyridine-1(2H)-carboxylate → Tert-butyl 4-(3-(4-(pyridin-2-ylamino)phenoxy)pyrazin-2-yl)piperidine-1-carboxylate

https://huagongshe.com/reaction/473708

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl 4-(3-(4-(pyridin-2-ylamino)phenoxy)pyrazin-2-yl)-5,6-dihydropyridine-1(2H)-carboxylateHCID 59374036—
CatalystPalladium hydroxideHCID 9942167—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 4-(3-(4-(pyridin-2-ylamino)phenoxy)pyrazin-2-yl)piperidine-1-carboxylateHCID 59374121—

Reaction Steps

To a N2 purged flask containing tert-butyl 4-(3-(4-(pyridin-2-ylamino)phenoxy)pyrazin-2-yl)-5,6-dihydropyridine-1(2H)-carboxylate (10.0 g, 22.45 mmol) and pearlman's catalyst (4.1 g, 5.84 mmol) was added THF (350 mL). H2 was bubbled through the solution for 4 minutes, then the solution was capped with a balloon of H2. After 48 hours, LC-MS shows complete conversion. The solution was filtered over a pad of celite, and the celite washed with EtOAc (150 mL). The filtrate was concentrated in vacuo. The residue was taken up in DCM (50 mL) and loaded onto a plug of silica gel (800 mL frit) and eluted with 0% to 50% EtOAc in hexanes to give tert-butyl 4-(3-(4-(pyridin-2-ylamino)phenoxy)pyrazin-2-yl)piperidine-1-carboxylate as a light yellow foam. MS (ESI, pos. ion) m/z: 448.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637500B2
Source datasetuspto-grants-2014_01
ORD IDord-f5614caebba34f2488b0b2a889dec4ae
Source noteuspto-grants-2014_01