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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2391558Generated: November 2, 2026

2-Aminophenol → HCID 57441062, compound

https://huagongshe.com/reaction/2391558

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminophenolHCID 5801—
ReactantPotassium CarbonateHCID 11430—
ReactantN-methyl-2-pyrrolidoneHCID 13387—
ReactantImidazo(1,2-b)pyridazine, 6-chloro-HCID 138828—
SolventSodium HydroxideHCID 14798—
ProductHCID 57441062HCID 5744106214%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 6-chloroimidazo[1,2-b]pyridazine (1536 mg, 10.0 mmol), 2-aminophenol (1419 mg, 13.0 mmol), potassium carbonate (4146 mg, 30.0 mmol) and N-methylpyrrolidone (10 mL) was stirred at 120° C. for 3 days. The reaction mixture was diluted with 1N aqueous sodium hydroxide solution and extracted with ethyl acetate. The organic layer was concentrated under reduced pressure, and the residue was purified by NH silica gel column chromatography (hexane/ethyl acetate=70/30→0/100). The objective fraction was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/methanol=100/0→75/25), and precipitated from diisopropyl ether to give the title compound (307 mg, 1.4 mmol, yield 14%) as a pale-brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273741B2
Source datasetuspto-grants-2012_09
ORD IDord-a6cc52d4c82746a8ad494c02370057a4
Source noteuspto-grants-2012_09