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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2391562Generated: October 30, 2026

Aniline → 2-(imidazo[1,2-b]pyridazin-6-ylthio)-N-phenylbenzamide

https://huagongshe.com/reaction/2391562

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantTriethylamineHCID 8471—
ReactantSodium HydroxideHCID 14798—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Reactant2-(Imidazo[1,2-b]pyridazin-6-ylthio)benzoic acidHCID 57441064—
SolventDimethylformamideHCID 6228—
Product2-(imidazo[1,2-b]pyridazin-6-ylthio)-N-phenylbenzamideHCID 5750578380%

Reaction Steps

To a mixture of 2-(imidazo[1,2-b]pyridazin-6-ylthio)benzoic acid (109 mg, 0.40 mmol), aniline (75 mg, 0.81 mmol), 1-hydroxybenzotriazole hydrate (61 mg, 0.40 mmol) and N,N-dimethylformamide (5 mL) were added 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride (153 mg, 0.80 mmol) and triethylamine (0.167 mL, 1.20 mmol), and the mixture was stirred at room temperature for 18 hr. A 1N aqueous sodium hydroxide solution was added to the mixture and the mixture was extracted with ethyl acetate. The organic layer was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/methanol=100/0→80/20) and precipitated from ethyl acetate/diisopropyl ether to give the title compound (110 mg, 0.32 mmol, yield 79%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273741B2
Source datasetuspto-grants-2012_09
ORD IDord-49b0b72b4a8f44b0b9b1c2797244f349
Source noteuspto-grants-2012_09