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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1046573Generated: October 30, 2026

Methyl iodide → 1,4-Di-tert-butyl 2-methyl (2S)-piperazine-1,2,4-tricarboxylate

https://huagongshe.com/reaction/1046573

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 40419050HCID 40419050—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product1,4-Di-tert-butyl 2-methyl (2S)-piperazine-1,2,4-tricarboxylateHCID 57356952116.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of solution of (S)-1,4bis(tert-butoxycarbonyl)piperazine-2-carboxylic acid (18.3 g, 45 mmol) and potassium carbonate (8.2 g; 59 mmol) in DMF (150 ml) cooled to 0° C. under N2, was added dropwise a solution of iodomethane (7.36 ml; 118 mmol). The reaction mixture was left to stir at room temperature for 18 h. It was diluted with ethyl acetate, washed with water and brine. The organic was dried over magnesium sulfate, filtered and concentrated under reduced pressure to afford the title compound as a white solid (18 g; 95%). 1H NMR (CDCl3) 1.46-1.50 (18H, d), 1.65 (3H, s), 2.80-2.90 (1H, m), 3.10-3.40 (2H, m), 3.75-4.10 (2H, m), 4.60-4.70 (2H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569337B2
Source datasetuspto-grants-2013_10
ORD IDord-b2f9b452875c4f85bdad4c23d82b9be8
Source noteuspto-grants-2013_10