HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 359436Generated: October 26, 2026
Ammonium Hydroxide → 3-(4-Ethylphenoxy)-6-[4-(3-methylphenyl)-1-piperazinyl]pyridazine
https://huagongshe.com/reaction/359436
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 1-(m-Tolyl)piperazine | HCID 83111 | — |
| Reactant | 6-Chloro-3-(4-ethylphenoxy)pyridazine | HCID 19095610 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 3-(4-Ethylphenoxy)-6-[4-(3-methylphenyl)-1-piperazinyl]pyridazine | HCID 15124606 | 27% |
Reaction Steps
A mixture of 4 parts of 6-chloro-3-(4-ethylphenoxy)pyridazine and 6 parts of 1-(3-methylphenyl)piperazine was stirred and heated for 3 hours in an oil bath at 110° C. The whole was alloWed to stand overnight. Concentrate ammonium hydroxide and trichloromethane were added. The precipitate was filtered off and the filtrate was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from 2,2'-oxybispropane. The product was filtered off and dried, yielding 1.7 parts (27%) of 3-(4-ethylphenoxy)-6-[4-(3-methylphenyl)-1-piperazinyl]pyridazine; mp. 106.6° C. (compound 221).
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-df627013c6d34e0b8b6a218a80ad02e3 |
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| Source note | uspto-grants-1991_03 |
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