HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1068007Generated: October 31, 2026
m-Chloroperbenzoic acid → N-[(4-chlorophenyl)methyl]-1-(3-methylsulfinylpropyl)-6-(morpholinomethyl)-4-oxo-quinoline-3-carboxamide
https://huagongshe.com/reaction/1068007
Participants
| Role | Name | HCID | Charge |
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| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | N-[(4-chlorophenyl)methyl]-1-(3-methylsulfanylpropyl)-6-(morpholinomethyl)-4-oxo-quinoline-3-carboxamide | HCID 16073877 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-[(4-chlorophenyl)methyl]-1-(3-methylsulfinylpropyl)-6-(morpholinomethyl)-4-oxo-quinoline-3-carboxamide | HCID 16073880 | 67.8% |
Reaction Steps
A solution of N-(4-chlorobenzyl)-1-[3-(methylsulfanyl)propyl]-6-(4-morpholinylmethyl)-4-oxo-1,4-dihydro-3-quinolinecarboxamide (0.10 gm) from Example No. 61 in dichloromethane (2 mL) at 0° C. is added p-toluenesulfonic acid hydrate (0.04 gm) followed by m-chloroperoxybenzoic acid (˜85%)(0.045 gm). The mixture is stirred for 0.5 hrs. The reaction mixture is diluted with dichloromethane, washed with saturated aqueous sodium sulfite, saturated aqueous sodium bicarbonate, brine, dried (Na2SO4) and concentrated under reduced pressure. The crude product is purified by flash column chromatography eluting with 3% to 9% methanol in dichloromethane. The product fractions are combined and recrystallized from ethyl acetate-methanol-hexanes to afford 0.07 gm of the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06248739B1 |
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| Source dataset | uspto-grants-2001_06 |
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| ORD ID | ord-cfb64910d6fb443ba511e62990da20cc |
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| Source note | uspto-grants-2001_06 |
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