HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 612159Generated: October 27, 2026
Sodium Carbonate → 4-(4-Chloro-2-fluoro-5-hydroxy-phenylamino)-6,7,8-trimethoxy-quinoline-3-carbonitrile
https://huagongshe.com/reaction/612159
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 5-Amino-2-chloro-4-fluorophenol | HCID 158654 | — |
| Reactant | Methylcarbonate | HCID 4585885 | — |
| Reactant | 1-Ethoxyethanol | HCID 10129898 | — |
| Reactant | 4-Chloro-6,7,8-trimethoxy-3-quinolinecarbonitrile | HCID 22466611 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(4-Chloro-2-fluoro-5-hydroxy-phenylamino)-6,7,8-trimethoxy-quinoline-3-carbonitrile | HCID 22466624 | — |
Reaction Steps
A mixture of 0.279 g of 4-chloro-6,7,8-trimethoxy-3-quinolinecarbonitrile, 0.22 g of the methyl carbonate of 4-chloro-2-fluoro-5-hydroxy-aniline, and 15 ml of ethoxy-ethanol was stirred under nitrogen, at reflux temperature for 30 minutes. The mixture was cooled and added to 100 ml of water. To this mixture was added sodium carbonate to pH 9. The product was collected, washed with water, and dried. The solids thus obtained were dissolved in a mixture of 30 ml of methyl alcohol and 20 ml of acetone. To this mixture was added 1.5 ml of 28-30% ammonium hydroxide solution. The mixture was heated at 50° C. for 30 minutes and concentrated. The product was collected, washed with ethyl acetate, and dried to give 0.162 g of 4-(4-chloro-2-fluoro-5-hydroxy-phenylamino)-6,7,8-trimethoxy-quinoline-3-carbonitrile as a solid, mp 223-225° C.; mass spectrum (EI, m/e): M 403.0731.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06002008 |
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| Source dataset | uspto-grants-1999_12 |
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| ORD ID | ord-9b0f59a9c5224ce9a4ece0e856e5b7b3 |
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| Source note | uspto-grants-1999_12 |
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