HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 580540Generated: October 31, 2026
Hydrochloric Acid → HCID 20133950, compound
https://huagongshe.com/reaction/580540
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 3-Chloro-6-methoxypyridazine | HCID 74403 | — |
| Reactant | HCID 20133992 | HCID 20133992 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 20133950 | HCID 20133950 | — |
Reaction Steps
4.0 g (0.06 mole) of 85% KOH are added to 8.7 g (0.03 mole) of 1,3-dimethyl-5-(4-hydroxyphenylcarbamoyl)barbituric acid in 70 ml of toluene and 50 ml of dimethyl sulfoxide. The mixture is dewatered with a water separator at reflux temperature. After the toluene has been distilled off, 4.3 g (0.03 mole) of 3-chloro-6-methoxypyridazine are added. The bath temperature is increased gradually until a temperature in the range from 120° to 140° C. is reached, and the mixture is kept at this temperature for 2 hours. The mixture is then cooled to 80° C., neutralised with dilute hydrochloric acid, cooled to room temperature and diluted with water. The precipitate is isolated by filtration, washed with water and dried.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04753940 |
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| Source dataset | uspto-grants-1988_06 |
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| ORD ID | ord-695829cf598e466c933a631c6720cafa |
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| Source note | uspto-grants-1988_06 |
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