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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175827Generated: November 1, 2026

tert-butyl (3S)-3-(hydroxymethyl)piperazine-1-carboxylate → (3S)-tert-butyl 4-(2-(3-cyano-4-fluoro-2-methylphenyl)-2-hydroxyethyl)-3-(hydroxymethyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/2175827

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl (3S)-3-(hydroxymethyl)piperazine-1-carboxylateHCID 24820294—
Reactant6-Fluoro-2-methyl-3-(oxiran-2-yl)benzonitrileHCID 86647307—
SolventEthanolHCID 702—
Product(3S)-tert-butyl 4-(2-(3-cyano-4-fluoro-2-methylphenyl)-2-hydroxyethyl)-3-(hydroxymethyl)piperazine-1-carboxylateHCID 71272768—

Reaction Conditions

Temperature150 °C

Reaction Steps

A mixture of 6-fluoro-2-methyl-3-(oxiran-2-yl)benzonitrile (785 mg, 4.43 mmol) and (S)-tert-butyl 3-(hydroxymethyl)piperazine-1-carboxylate (1340 mg, 6.2 mmol) in ethanol (10 mL) was heated in microwave at 150° C. for 3 h. The volatile was evaporated and the residue was purified on Biotage using 40-100% ethyl acetate/hexane to give the title compound: LC/MS: (M+1)+: 394.19.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062070B2
Source datasetuspto-grants-2015_06
ORD IDord-2a7bf4f707bc40ce95b65abee3a73df2
Source noteuspto-grants-2015_06