HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341060Generated: October 26, 2026
Potassium Phosphate, Tribasic → 2-(2-Fluorophenyl)-5-{[5-(4-methyl-1H-imidazol-1-yl)pyridin-2-yl]methyl}-2,5-dihydro-3H-pyrazolo[4,3-c]quinolin-3-one
https://huagongshe.com/reaction/341060
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | trans-N,N'-dimethyl-1,2-cyclohexanediamine | HCID 2733821 | — |
| Reactant | 5-[(5-Bromopyridin-2-yl)methyl]-2-(2-fluorophenyl)-2,5-dihydro-3H-pyrazolo[4,3-c]quinolin-3-one | HCID 68154492 | — |
| Reactant | HCID 178418800 | HCID 178418800 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(2-Fluorophenyl)-5-{[5-(4-methyl-1H-imidazol-1-yl)pyridin-2-yl]methyl}-2,5-dihydro-3H-pyrazolo[4,3-c]quinolin-3-one | HCID 52914607 | — |
Reaction Steps
5-[(5-Bromopyridin-2-yl)methyl]-2-(2-fluorophenyl)-2,5-dihydro-3H-pyrazolo[4,3-c]quinolin-3-one [(Example 257, Step 1), 0.13 g, 030 mmol], 4-methyl-1H-imidazole (99 mg, 1.2 mmol, 4 equiv), copper(I) iodide (23 mg, 0.12 mmol, 0.4 equiv), (±)-trans-N,N′-dimethylcyclohexane-1,2-diamine (34 mg, 0.24 mmol, 0.8 equiv) and potassium phosphate (0.19 g, 0.90 mmol, 3 equiv) were combined in water (0.2 mL) and dimethylsulfoxide (1 mL). The mixture was sparged under an atmosphere of nitrogen, the vessel was sealed and placed into a preheated oil bath at 100° C. for 9 hours. The mixture was cooled to ambient temperature, poured into water (25 mL) and extracted with chloroform (2×25 mL). The combined organic extracts were washed with water (20 mL) and brine (20 mL), dried with sodium sulfate, filtered and concentrated in vacuo. The residue was purified by silica gel gradient chromatography (100:0 to 96:4; chloroform:methanol), providing the titled compound: 1H-NMR (400 MHz, CDCl3) δ 8.70 (1H, d, J=2.7 Hz), 8.55 (1H, s), 8.42 (1H, d, J=7.2 Hz), 7.76 (1H, s), 7.67-7.63 (2H, m), 7.56-7.47 (3H, m), 7.39-7.31 (2H, m), 7.29-7.23 (2H, m), 7.00 (1H, s), 5.59 (2H, s), 2.30 (3H, s) ppm; high resolution mass spectrometry (ES+) m/z 451.1653 [(M+H)+; calculated for C26H20FN6O: 451.1677].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08895580B2 |
|---|
| Source dataset | uspto-grants-2014_11 |
|---|
| ORD ID | ord-d5a6aca596bf4d8b9d06feb58c1b72ba |
|---|
| Source note | uspto-grants-2014_11 |
|---|