HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1414869Generated: October 31, 2026
Sodium Chloride → Carbazic acid, 3-(6-((2-hydroxyethyl)methylamino)pyridazin-3-YL)-, ethyl ester
https://huagongshe.com/reaction/1414869
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Hydrazinecarboxylic acid, ethyl ester | HCID 20064 | — |
| Reactant | 2-[(6-Chloropyridazin-3-yl)(methyl)amino]ethan-1-ol | HCID 12237589 | — |
| Solvent | Water | HCID 962 | — |
| Product | Carbazic acid, 3-(6-((2-hydroxyethyl)methylamino)pyridazin-3-YL)-, ethyl ester | HCID 41014 | — |
Reaction Steps
A mixture of 1.87 g (0.01 moles) 3-chloro-6-[N-(2-hydroxyethyl)-methylamino]-pyridazine and 2.08 g (0.02 moles) monocarbethoxyhydrazine is warmed up to 155° C and kept at this temperature for half an hour. The product is cooled and dissolved in water, alkalinized by addition of solid potassium carbonate and the aqueous solution saturated by adding sodium chloride. A flocky precipitate separates which is subsequently collected by filtration and crystallized from ethanol, to give with good yields 3-(2-carbethoxyhydrazino)-6-[N-(2-hydroxyethyl)methylamino] -pyridazine melting at 131°-133° C. I.R. Spectrum (mineral oil, cm-1); 3320-3080 (OH and NH), 1715 (C=O carbamate), 1500 (pyridazinic ring), 840 (two ortho aromatic hydrogens).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04002753 |
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| Source dataset | uspto-grants-1977_01 |
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| ORD ID | ord-8be1f7af65f142aa9d65090498c24b6d |
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| Source note | uspto-grants-1977_01 |
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