HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 215824Generated: October 30, 2026
Potassium Iodide → HCID 25119537, compound
https://huagongshe.com/reaction/215824
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 58337192 | HCID 58337192 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 25119537 | HCID 25119537 | 38.2% |
Reaction Steps
A mixture of 7-[4-(3-chloropropylsulfonyloxy)-2-methoxyphenyl]-8-(5-fluoro-2-methylphenoxymethyl)-1,3,3-trimethyl-3,4-dihydro-1H-quinoxalin-2-one (Reference Compound No. 1-54, 50.0 mg, 0.0846 mmol), benzylamine (92.4 μL, 0.846 mmol), and potassium iodide (16.9 mg, 0.102 mmol) was suspended in anhydrous N,N-dimethylformamide (0.4 mL) and stirred at 50° C. for 5 hours. After cooling down, ethyl acetate (50 mL) was added thereto. The organic layer was washed with water (50 mL) and saturated brine (30 mL), dried over anhydrous magnesium sulfate, and then the solvent was removed under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give the titled compound (21.4 mg) as a colorless amorphous product. (Yield 38%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08193187B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-3cedc1e65e18478880e39d68ab5e6973 |
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| Source note | uspto-grants-2012_06 |
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