HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582982Generated: November 1, 2026
1,1-Dichloroethane → HCID 12988030, compound
https://huagongshe.com/reaction/1582982
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,1-Dichloroethane | HCID 6365 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 22716704 | HCID 22716704 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 12988030 | HCID 12988030 | 26.6% |
Reaction Steps
To a 10 ml dichloroethane solution containing 630 mg of 3-(3-aminopropyl)-4-(3-chlorophenyl)-l-ethyl-7-methyl-1,8-naphthyridin-2(1H)-one were added 243 mg of methanesulfonyl chloride and 0.30 ml of triethylamine under ice cooling, followed by stirring for 1 hour with warming to room temperature. The reaction mixture was diluted with ethyl acetate and washed with saturated sodium bicarbonate aqueous solution and saturated brine. The solvent was evaporated from the organic layer and the resulting residue was purified by a silica gel column chromatography (hexane-ethyl acetate) and then recrystallized from ethanol-water to obtain 204 mg of N-{3-[4-(3-chlorophenyl)-1-ethyl-7-methyl-2-oxo-1,2-dihydro-1,8-naphthyridin-3-yl]propyl}methanesulfonamide as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06740662B1 |
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| Source dataset | uspto-grants-2004_05 |
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| ORD ID | ord-78cdc012a9b446a897ae14f068adffd5 |
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| Source note | uspto-grants-2004_05 |
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