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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473713Generated: October 26, 2026

Water → Tert-butyl 4-(3-(4-(5-methylpyridin-2-ylamino)phenoxy)pyrazin-2-yl)piperidine-1-carboxylate

https://huagongshe.com/reaction/473713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium t-butoxideHCID 23676156—
ReactantTert-butyl 4-(3-fluoropyrazin-2-yl)piperidine-1-carboxylateHCID 59351396—
Reactant4-(5-Methylpyridin-2-ylamino)phenolHCID 59373986—
SolventDimethyl SulfoxideHCID 679—
ProductTert-butyl 4-(3-(4-(5-methylpyridin-2-ylamino)phenoxy)pyrazin-2-yl)piperidine-1-carboxylateHCID 59373921—

Reaction Steps

A mixture of tert-butyl 4-(3-fluoropyrazin-2-yl)piperidine-1-carboxylate (9.55 mL, 3.73 mmol), 4-(5-methylpyridin-2-ylamino)phenol (0.747 g, 3.73 mmol), and sodium tert-butoxide (1.07 g, 11.20 mmol) in DMSO (15 mL) was stirred at RT in 24 h. Water was added, and the reaction mixture was extracted with ether (3×), dried over MgSO4, concentrated and purified by ISCO (0-60% EtOAc/Hexanes) to give the light brown oil. MS (ESI, pos. ion) m/z: 462.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637500B2
Source datasetuspto-grants-2014_01
ORD IDord-fb54f3d6ab464d388278e2f5d350c3f5
Source noteuspto-grants-2014_01