HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 569914Generated: October 27, 2026
Hydrochloric Acid → HCID 20146592, compound
https://huagongshe.com/reaction/569914
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methylhydrazine | HCID 6061 | — |
| Reactant | 1,5,6,7-Tetrahydro-5-(hydroxymethylene)-1-methyl-4h-indazol-4-one | HCID 57162714 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 20146592 | HCID 20146592 | 51% |
Reaction Steps
A solution of 3.2 ml of methylhydrazine in 30 ml of methanol was added dropwise to an ice-cold solution of 10.5 g of 1,5,6,7-tetrahydro-5-hydroxymethylene-1-methyl-4H-indazol-4-one in 200 ml of methanol. The reaction was heated at reflux for 3.5 hours and the solvent was then removed under reduced pressure. The residue was triturated with a mixture of ether and ethanol to give a crude tan solid. This solid was dissolved in a mixture of ether and ethanol and acidified with ethereal hydrogen chloride. The yellow precipitate which formed was separated by filtration and recrystallized from a mixture of ethanol and propanol to give 1,4,5,6-tetrahydro-1,6-dimethylbenzo[1,2-c:3,4-c']dipyrazole monohydrochloride as a yellow crystalline solid melting at about 222°-226° C. with decomposition (51% yield). This compound has the following structural formula: ##STR6##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04734430 |
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| Source dataset | uspto-grants-1988_03 |
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| ORD ID | ord-a80dd788797c4fd3a3a655bf6734bdd7 |
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| Source note | uspto-grants-1988_03 |
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