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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1502014Generated: October 29, 2026

tert-Butyl (3R)-3-(hydroxymethyl)piperazine-1-carboxylate → (3R)-tert-butyl 4-(2-(3-cyano-2,4-difluorophenyl)-2-hydroxyethyl)-3-(hydroxymethyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1502014

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl (3R)-3-(hydroxymethyl)piperazine-1-carboxylateHCID 24820286—
Reactant2,6-Difluoro-3-(oxiran-2-yl)benzonitrileHCID 86727061—
SolventEthanolHCID 702—
Product(3R)-tert-butyl 4-(2-(3-cyano-2,4-difluorophenyl)-2-hydroxyethyl)-3-(hydroxymethyl)piperazine-1-carboxylateHCID 86727064—

Reaction Steps

2,6-difluoro-3-(oxiran-2-yl)benzonitrile (3.70 g, 20.4 mmol) and (R)-tert-butyl 3-(hydroxymethyl)piperazine-1-carboxylate (6.63 g, 30.6 mmol) were dissolved in ethanol (36.0 mL) then placed in 3-20 mL sealed tubes and microwaved at 140° C. for 1 h. The solvents were evaporated and the combined residue was purified by chromatography through a 120 g ISCO Redi-sep column with 50% to 100% ethyl acetate/hexane solvent system to yield the title compound LC-MS (IE, m/z): 398 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206199B2
Source datasetuspto-grants-2015_12
ORD IDord-bdb425e1391f4369999f0cec3910f382
Source noteuspto-grants-2015_12