HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 43373Generated: October 26, 2026
Water → (2S)-2-Methyl-1-[(6-methyl-3-pyridinyl)carbonyl]piperazine
https://huagongshe.com/reaction/43373
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 6-Methylnicotinic acid | HCID 137860 | — |
| Reactant | Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 2733084 | — |
| Reactant | (S)-1-Boc-3-methylpiperazine | HCID 7023035 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (2S)-2-Methyl-1-[(6-methyl-3-pyridinyl)carbonyl]piperazine | HCID 59161378 | 1,394.9% |
Reaction Steps
To a solution of 1,1-dimethylethyl (3S)-3-methyl-1-piperazinecarboxylate (1 g, 4.99 mmol) in DMF (5 ml) was added 6-methyl-3-pyridinecarboxylic acid (0.685 g, 0.340 mmol), HOBT.H2O (0.765 g, 4.99 mmol) and HBTU (1.894 g, 4.99 mmol). Finally DIPEA (2.62 ml, 14.98 mmol) was added and the reaction mixture was stirred at room temperature for 20 hours. Solvent was removed by evaporation and EtOAc was added to the residue and the solution was extracted with saturated aqueous sodium bicarbonate and sodium chloride solutions. The organic layer was evaporated to dryness and dissolved in dioxane (100 ml) and stirred with 4M HCl in dioxane (15 ml) and water (0.25 ml) overnight. The solution was evaporated to dryness and purified using an ion exchange column (SCX, Biotage) to give the title compound as an oil (1.04 g)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08536183B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-72d4c1c2e2d642058b9a80973bd0f26e |
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| Source note | uspto-grants-2013_09 |
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