HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466558Generated: October 29, 2026
Sodium Carbonate → HCID 15124730, compound
https://huagongshe.com/reaction/466558
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 3,6-Dichloropyridazine | HCID 67331 | — |
| Reactant | HCID 19095529 | HCID 19095529 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 15124730 | HCID 15124730 | 16.8% |
Reaction Steps
A mixture of 4.5 parts of 3,6-dichloropyridazine, 4.9 parts of N-[3-(trifluoromethyl)phenyl]-3-piperidinamine, 6.4 parts of sodium carbonate and 180 parts of N,N-dimethylformamide was stirred overnight at about 65° C. The reaction mixture was poured into ice water and the product was extracted with dichloromethane. The extract was dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (99:1 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from 2-propanol. The product was filtered off (the filtrate was set aside) and dried, yielding 1.2 parts (16.8%) of 1-(6-chloro-3-pyridazinyl)-N-[3-(trifluoromethyl)phenyl]-3-piperidinamine; mp. 92.6° C. (compound 146). The filtrate, which was set aside, was converted into the hydrochloride salt in 2-propanol. The salt was filtered off and dried, yielding 2.6 parts (32.9%) of 1-(6-chloro-3-pyridazinyl)-N-[3-(trifluoromethyl)phenyl[-3-piperidinamine monohydrochloride; mp. 173.5° C. (compound 147).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05157035 |
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| Source dataset | uspto-grants-1992_10 |
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| ORD ID | ord-079078863b45478997f67908d15d7e91 |
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| Source note | uspto-grants-1992_10 |
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