HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 717592Generated: October 30, 2026
Methyl iodide → 1,4-Di-tert-butyl 2-methyl (2S)-piperazine-1,2,4-tricarboxylate
https://huagongshe.com/reaction/717592
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 40419050 | HCID 40419050 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1,4-Di-tert-butyl 2-methyl (2S)-piperazine-1,2,4-tricarboxylate | HCID 57356952 | 116.1% |
Reaction Steps
To a suspension of solution of (S)-1,4-bis(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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09193722B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-93d75ad28a134ce0bd23f3559f550dac |
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| Source note | uspto-grants-2015_11 |
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