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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239825Generated: October 26, 2026

4-Ethoxyaniline → 6-chloro-N-(4-ethoxyphenyl)-7-methylimidazo[1,2-b]pyridazin-8-amine

https://huagongshe.com/reaction/2239825

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-EthoxyanilineHCID 9076—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 86618518HCID 86618518—
SolventTetrahydrofuranHCID 8028—
Product6-chloro-N-(4-ethoxyphenyl)-7-methylimidazo[1,2-b]pyridazin-8-amineHCID 86611715—

Reaction Steps

(1d variation 2) To a mixture of bromo-6-chloro-7-methylimidazo[1,2-b]pyridazine HCl salt (102 mg, 0.36 mmol) from 1c, in THF (1.5 ml) was added p-Phenetidine (49 mg, 0.36 mmol) and a 1.0 M solution of KOt-Bu in THF (3.0 eq, 1.08 ml, 1.08 mmol). The mixture was allowed to heat at 50 C for 1 hour. The solution was then concentrated in vacuo to dryness to provide 6-chloro-N-(4-ethoxyphenyl)-7-methylimidazo[1,2-b]pyridazin-8-amine as a solid. m/e 303 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723336B2
Source datasetuspto-grants-2010_05
ORD IDord-839f6f10943b41999956984bbe293e7f
Source noteuspto-grants-2010_05