HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333966Generated: October 30, 2026
Diisopropylethylamine → N,2,6-trimethyl-4-[4-[(E)-4,4,4-trifluorobut-2-enoyl]piperazin-1-yl]pyridine-3-carboxamide
https://huagongshe.com/reaction/333966
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 2733084 | — |
| Reactant | 4,4,4-Trifluorocrotonic acid | HCID 5709614 | — |
| Reactant | N,2,6-Trimethyl-4-piperazin-1-yl-pyridine-3-carboxamide | HCID 66835676 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N,2,6-trimethyl-4-[4-[(E)-4,4,4-trifluorobut-2-enoyl]piperazin-1-yl]pyridine-3-carboxamide | HCID 56949085 | 38.7% |
Reaction Steps
(E)-4,4,4-Trifluorobut-2-enoic acid (21 mg, 0.15 mmol) was dissolved in anhydrous DMF (1 ml), diisopropylethylamine (52 μl, 0.3 mmol) was added followed by HBTU (60 mg, 0.15 mmol) and the mixture was stirred at room temperature for 15 minutes. N,2,6-trimethyl-4-piperazin-1-yl-pyridine-3-carboxamide (37.2 mg, 0.15 mmol) was dissolved in a mixture of DMF (0.5 ml) and diisopropylethylamine (26 μl, 0.15 mmol) and the resulting solution was added to the solution of the activated carboxylic acid. The resulting mixture was stirred at room temperature for three hours, the solvent was removed under reduced pressure and the raw product was purified by preparative HPLC (gradient of water containing 0.1% ammonia and acetonitrile) to yield 21.4 mg of a solid (0.058 mmol, 38%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08883791B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-da8c88080e1e4ecb9c1f83c0f938030d |
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| Source note | uspto-grants-2014_11 |
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