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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantPotassium CarbonateHCID 11430—
ReactantHydrazinecarboxylic acid, ethyl esterHCID 20064—
Reactant2-[(6-Chloropyridazin-3-yl)(methyl)amino]ethan-1-olHCID 12237589—
SolventWaterHCID 962—
ProductCarbazic acid, 3-(6-((2-hydroxyethyl)methylamino)pyridazin-3-YL)-, ethyl esterHCID 41014—

Reaction Conditions

Temperature155 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04002753
Source datasetuspto-grants-1977_01
ORD IDord-8be1f7af65f142aa9d65090498c24b6d
Source noteuspto-grants-1977_01