HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1369423Generated: October 31, 2026
Triethylamine hydrochloride → HCID 22609916, compound
https://huagongshe.com/reaction/1369423
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine hydrochloride | HCID 11130 | — |
| Reactant | 2,4-Difluorobenzoic acid hydrazide | HCID 2736922 | — |
| Reactant | HCID 22609937 | HCID 22609937 | — |
| Solvent | P-Xylene | HCID 7809 | — |
| Product | HCID 22609916 | HCID 22609916 | 38.7% |
Reaction Steps
A mixture of 3,6-dichloro-4-(1-methylcyclohexyl)pyridazine (1.29 g, 5.27 mmol), 2,4-difluorobenzoic hydrazide (1.72 g, 10 mmol) and triethylamine hydrochloride (1.09 g, 7.9 mmol) in p-xylene (5 ml) was stirred and heated at reflux for 24 hours. Upon cooling, the volatiles were removed in vacuo and the residue was partitioned between dichloromethane (100 ml) and water (100 ml) and NaHCO3 (100 ml). Undissolved solid was removed by filtration. The layers were separated and the aqueous was further extracted with dichloromethane (2×100 ml). The combined organic extracts were dried (MgSO4), filtered and evaporated. The residue was purified by chromatography on silica eluting with 0%→25% ethyl acetate in dichloromethane to give the required product (0.74 g): 1H NMR (250 MHz, CDCl3) δ1.34-1.74 (6H, m), 1.50 (3H, s), 1.90-2.15 (4H, m), 7.01-7.14 (2H, m), 7.87-7.98 (1H, m), 8.18 (1H, s); MS (ES+) m/e 365 [MH]+, 363 [MH]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06579875B1 |
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| Source dataset | uspto-grants-2003_06 |
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| ORD ID | ord-23d850436baf44e8848985867fb109b9 |
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| Source note | uspto-grants-2003_06 |
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