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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1451292Generated: October 31, 2026

Hydrazine hydrate (1:1) → HCID 178418284, compound

https://huagongshe.com/reaction/1451292

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantHCID 178418327HCID 178418327—
SolventEthanolHCID 702—
ProductHCID 178418284HCID 178418284112.8%

Reaction Steps

To a stirred suspension of dimethyl 4-hydroxyquinoline-2,3-dicarboxylate (1.00 g, 3.83 mM, prepared as described by H. Biere and W. Seelen, Liebigs Ann. Chem. 1976, 1972) in ethanol (15 mL) was added hydrazine hydrate (9.64 g, 193 mM) whereupon the solids dissolved. The resulting solution was refluxed for 3 hr during which time a thick precipitate formed. The cooled reaction mixture was filtered and the collected yellow solids were washed with ethanol and then ether. Air drying provided 0.99 g of the hydrazine salt of 2,3-dihydro-10-hydroxypyridazino [4,5-b]quinoline-1,4-dione. This material was boiled in glacial acetic acid (40 mL) and, after cooling to room temperature, the mixture was filtered. The collected solids were washed with several portions of ethyl acetate and then ether. Air drying provided the title pyridazinodione (0.72 g, 82%) as a yellow solid, mp >400° C.; Mass Spectrum (Chemical Ionization): 230 (M+H). Analysis for C11H7N3O3 : Calculated: C, 57.65; H, 3.08; N, 18.33 Found: C, 57.54; H, 3.26; N, 18.64

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05604227
Source datasetuspto-grants-1997_02
ORD IDord-00bfa08341ab40e49ea216e546623425
Source noteuspto-grants-1997_02