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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 427334Generated: October 30, 2026

Triethylamine → HCID 18357032, compound

https://huagongshe.com/reaction/427334

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Furancarbonyl chlorideHCID 68242—
ReactantHCID 22288370HCID 22288370—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 18357032HCID 1835703228.2%

Reaction Steps

Triethylamine (1.46 ml, 10.5 mmol) and 2-furoyl chloride (1.03 ml, 10.4 mmol) were added to a stirred solution of 1-chloro-4-hydrazinophthalazine hydrochloride (2.0 g, 8.7 mmol) in dioxane (200 ml) at room temperature under nitrogen. The mixture was stirred at room temperature for 2 h and then heated at reflux for 6 h. The mixture was cooled to room temperature, the solvent evaporated in vacuo and the residue partitioned between dichloromethane (800 ml) and water (200 ml). The organic layer was separated, washed further with water (4×200 ml) and brine (x 1), dried (MgSO4) and evaporated in vacuo. The residue was chromatographed on silica gel, eluting with a 0.5-2% methanol/dichloromethane gradient, to afford the title-product (0.665 g, 28%); 1H NMR (250 MHz, CDCl3) 6.68 (1H, q, J=1.7 Hz, Ar—H), 7.56 (1H, m, Ar—H), 7.73 (1H, m, Ar—H), 7.91 (1H, m, Ar—H), 8.05 (1H, m, Ar—H), 8.31 (1H, d, J=7.5 Hz, Ar—H), 8.76 (1H, m, Ar—H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06313125B1
Source datasetuspto-grants-2001_11
ORD IDord-1950a3be517848dd9c135e73110a7da0
Source noteuspto-grants-2001_11