HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750147Generated: October 28, 2026
Sodium Iodide → 7-(5-(4-(2-methoxyphenyl)piperazin-1-yl)pentyloxy)-3,4-dihydroquinolin-2(1H)-one
https://huagongshe.com/reaction/1750147
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-(2-Methoxyphenyl)piperazine hydrochloride | HCID 9899402 | — |
| Reactant | 7-(4-(4-(2,3-dichlorophenyl)-1,4-diazepan-1-yl)butoxy)quinolin-2(1H)-one | HCID 66559588 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 7-(5-(4-(2-methoxyphenyl)piperazin-1-yl)pentyloxy)-3,4-dihydroquinolin-2(1H)-one | HCID 56664952 | 81% |
Reaction Steps
A mixture of intermediate 4 (110 mg, 0.34 mmol) and NaI (102 mg, 1.36 mmol) in CH3CN was heated to reflux for 30 min and then cooled to rt. Intermediate 55 (117 mg, 0.51 mmol) and anhydrous K2CO3 (188 mg, 1.36 mmol) were added to the mixture. The resulting mixture was heated to reflux and stirred for 4 h. Precipitated crystals were filtered off and the filtrate was evaporated under reduced pressure. The residue was extracted with EtOAc. The combined EtOAc layers were washed with brine, dried over anhydrous Na2SO4, concentrated in vacuo and purified by flash chromatography on silica gel column (elution with DCM/MeOH=30:1) to give 7-(5-(4-(2-methoxyphenyl)piperazin-1-yl)pentyloxy)-3,4-dihydroquinolin-2(1H)-one (compound 39) (112 mg, 81%). 1H NMR (300 MHz, CDCl3): δ 7.92 (brs, 1H), 7.06-6.85 (m, 5H), 6.52 (d, J=6.6 Hz, 1H), 6.31 (s, 1H), 3.98-3.94 (m, 2H), 3.86 (s, 3H), 3.12 (br, 4H), 2.92-2.87 (m, 2H), 2.69-2.59 (m, 6H), 2.52-2.47 (m, 2H), 1.82-1.72 (m, 4H). HPLC: 99%, RT 2.100 min. MS (ESI) m/z 410.2 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09156822B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-bb981dae42af4c788791757294f961c9 |
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| Source note | uspto-grants-2015_10 |
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