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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2306583Generated: October 31, 2026

Triethylamine hydrochloride → HCID 22609916, compound

https://huagongshe.com/reaction/2306583

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamine hydrochlorideHCID 11130—
Reactant2,4-Difluorobenzoic acid hydrazideHCID 2736922—
ReactantHCID 22609937HCID 22609937—
SolventP-XyleneHCID 7809—
ProductHCID 22609916HCID 2260991638.7%

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) δ 1.34-1.74 (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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06828322B2
Source datasetuspto-grants-2004_12
ORD IDord-32af33f3d69c42888c0aea4b0ff0ce6a
Source noteuspto-grants-2004_12