HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 851525Generated: November 1, 2026
Hydrochloric Acid → HCID 20501555, compound
https://huagongshe.com/reaction/851525
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methylhydrazine | HCID 6061 | — |
| Reactant | 2,5-Hexanedione | HCID 8035 | — |
| Reactant | 3,6-Dichloropyridazine | HCID 67331 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 20501555 | HCID 20501555 | 59.2% |
Reaction Steps
A mixture of water (300 ml), 3,6-dichloropyridazine (29.8 g; 0.2 mole), methylhydrazine (9.2 g; 0.2 mole), and sodium bicarbonate (17.8 g; 0.2 mole), is heated to the reflux temperature for two hours. After cooling to about 60° C., acetonylacetone (22.2 g; 0.2 mole) is added and stirring is prosecuted for further 1 hour. Then the mixture is neutralized with hydrochloric acid and the obtained precipitate is collected and crystallized from ethyl ether, yielding 28 g (59.2%) of 6-chloro-N-(2,5-dimethyl-1H-pyrrol-1-yl)-N-methyl-3-pyridazineamine, whose structure is confirmed by I.R. and NMR spectra. M.p. 93°-94.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04385179 |
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| Source dataset | uspto-grants-1983_05 |
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| ORD ID | ord-046629c6c6284468b016c72af451f03e |
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| Source note | uspto-grants-1983_05 |
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