HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1756805Generated: November 2, 2026
Sodium Carbonate → 3-ethoxycarbonyl-6,7-difluoro-2-[N-methyl-N-(beta-aminocarbonylethyl)amino]quinoline
https://huagongshe.com/reaction/1756805
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-Chloro-3-ethoxycarbonyl-6,7-difluoroquinoline | HCID 9795461 | — |
| Reactant | N~3~-Methyl-beta-alaninamide | HCID 22182162 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-ethoxycarbonyl-6,7-difluoro-2-[N-methyl-N-(beta-aminocarbonylethyl)amino]quinoline | HCID 18994587 | 94.6% |
Reaction Steps
4.4 g of sodium carbonate are added to a solution of 4 g of 2-chloro-3-ethoxycarbonyl-6,7-difluoro-quinoline, prepared as described in Application Example 1, and 3 g of N-methyl-N-(b-aminocarbonylethyl)amine in 40 cm3 of toluene. The suspension obtained is heated to reflux and then stirred for 2 hours 30 minutes at this temperature. The reaction mixture is then cooled to approximately 20° C. and thereafter washed with 3 times 25 cm3 of water. The organic phase is concentrated to dryness under reduced pressure (20 kPa) at approximately 50° C. 4.7 g of 3-ethoxycarbonyl-6,7-difluoro-2-[N-methyl-N-(b-aminocarbonylethyl)amino]quinoline are obtained in the form of an oil, which is used without further purification for the subsequent steps.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05442070 |
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| Source dataset | uspto-grants-1995_08 |
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| ORD ID | ord-7708ac1b21994a70812b71fec0d6b38f |
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| Source note | uspto-grants-1995_08 |
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