HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1068028Generated: November 1, 2026
Dichloromethane → N-[(4-chlorophenyl)methyl]-1-[(4-chlorophenyl)sulfanylmethyl]-6-(morpholinomethyl)-4-oxo-quinoline-3-carboxamide
https://huagongshe.com/reaction/1068028
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Benzene, 1-chloro-4-((chloromethyl)thio)- | HCID 23610 | — |
| Reactant | HCID 178513551 | HCID 178513551 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-[(4-chlorophenyl)methyl]-1-[(4-chlorophenyl)sulfanylmethyl]-6-(morpholinomethyl)-4-oxo-quinoline-3-carboxamide | HCID 16073907 | — |
Reaction Steps
A suspension of N-(4-chlorobenzyl-4-hydroxy-6-(4-morpholinylmethyl)-3-quinolinecarboxamide (0.25 gm) from Preparation No. 40 and cesium carbonate (0.39 gm) in DMF (3 mL) is treated with chloromethyl 4-chlorophenyl sulfide (0.13 mL). The mixture is tightly capped and heated to 105° C. for 2 hrs. The reaction mixture is allowed to cool to room temperature, diluted with dichloromethane (50 mL), washed with water (2×10 mL), brine, dried (Na2SO4) and concentrated under reduced pressure. The crude product is purified by flash column chromatography eluting with 1% to 3% methanol in dichloromethane and then by trituration with ethyl acetate to afford 0.26 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-05c6bed423404959bb0ca97049edf8ce |
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| Source note | uspto-grants-2001_06 |
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