HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333928Generated: October 25, 2026
Diisopropylethylamine → (E)-1-[4-(2-Methoxy-4-quinolyl)piperazin-1-yl]-4-methyl-hept-2-en-1-one
https://huagongshe.com/reaction/333928
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | 4-Methylhept-2-enoic acid | HCID 21720203 | — |
| Reactant | 2-Methoxy-4-piperazin-1-yl-quinoline | HCID 66835874 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (E)-1-[4-(2-Methoxy-4-quinolyl)piperazin-1-yl]-4-methyl-hept-2-en-1-one | HCID 56948961 | 40% |
Reaction Steps
(E)-4-Methyl-hept-2-enoic acid (21.3 mg, 0.15 mmol) was dissolved in DMF (350 μl), diisopropylethylamine was added (26 μl, 0.15 mmol) followed by HATU (57 mg, 0.15 mmol dissolved in 0.25 ml DMF). The mixture was stirred at room temperature for 15 minutes, then 2-methoxy-4-piperazin-1-yl-quinoline (36.4 mg, 0.15 mmol, dissolved in 1 ml DMF) was added and stirring was continued overnight. The mixture was evaporated under reduced pressure, the residue was dissolved in dichloromethane and the resulting solution was washed with 5% sodium bicarbonate solution, water, evaporated to dryness under reduced pressure. The residue was purified by preparative HPLC (gradient of water containing 0.1% NH3 and acetonitrile) to yield 21.1 mg (0.06 mmol, 39.8%) of a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08883791B2 |
|---|
| Source dataset | uspto-grants-2014_11 |
|---|
| ORD ID | ord-32aec6e0d04d40cf81c859d5b8092f64 |
|---|
| Source note | uspto-grants-2014_11 |
|---|