HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 359447Generated: October 29, 2026
Hydrochloric Acid → HCID 178424551, compound
https://huagongshe.com/reaction/359447
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 178424721 | HCID 178424721 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178424551 | HCID 178424551 | 75% |
Reaction Steps
A mixture of 2.9 parts of 6-[4-hydroxy-4-(3-methylphenyl)-1-piperidinyl]-3-pyridazinol, 30 parts of a hydrochloric acid solution 6 N and 24 parts of ethanol was stirred for 2 hours at reflux temperature. The reaction mixture was evaporated. Crushed ice was added and the whole was treated with concentrate ammonium hydroxide. The product was extracted with trichloromethane The extract was dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (98:2 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from a mixture of 2-propanol and 2,2'-oxybispropane. The product was filtered off and dried, yielding 2 parts (75%) of 6-[3,6-dihydro-4-(3-methylphenyl)-1(2H)pyridinyl]-3-pyridazinol; mp. 179.0° C. (compound 270).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05001125 |
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| Source dataset | uspto-grants-1991_03 |
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| ORD ID | ord-46b94aeedde74bdc862edf16a51dafd3 |
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| Source note | uspto-grants-1991_03 |
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