HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582981Generated: November 2, 2026
HCID 12988027, compound → HCID 12988028, compound
https://huagongshe.com/reaction/1582981
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 12988027 | HCID 12988027 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 12988028 | HCID 12988028 | — |
Reaction Steps
A 720 mg portion of ethyl N-[4-(3-chlorophenyl)-1-ethyl-7-methyl-2-oxo-1,2-dihydro-1,8-naphthyridin-3-yl]carbamate was stirred in 40 ml of an ethanol-3M sodium hydroxide aqueous solution (1:1) under heating at an oil bath temperature of 100° C. for 4 hours. After cooling to room temperature, the reaction mixture was diluted with water and then extracted with ethyl acetate. The organic layer was washed with saturated brine and the solvent was evaporated. The resulting residue was purified by a silica gel column chromatography (toluene-ethyl acetate) and then recrystallized from diisopropyl ether-ethyl acetate to obtain 298 mg of 3-amino-4-(3-chlorophenyl)-1-ethyl-7-methyl-1,8-naphthyridin-2(1H)-one 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-e5007139015e4fbbb332ea1ad38b84d3 |
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| Source note | uspto-grants-2004_05 |
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