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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1909078Generated: October 27, 2026

Pyridine → Imidazo[1,2-b]pyridazin-3-yl-carbamic acid phenyl ester

https://huagongshe.com/reaction/1909078

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPhenyl chloroformateHCID 15891—
ReactantImidazo[1,2-b]pyridazin-3-amineHCID 10702308—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductImidazo[1,2-b]pyridazin-3-yl-carbamic acid phenyl esterHCID 5844268172%

Reaction Steps

To a solution of imidazo[1,2-b]pyridazin-3-ylamine (209 mg, 1.56 mmol) in dry DMF (5.0 mL) was added pyridine (382 μL, 4.68 mmol) and phenyl chloroformate (244 mg, 1.56 mmol). After 3 h at rt, the mixture was diluted with EtOAc (100 mL) and washed with saturated aqueous NaHCO3 (50 mL). The organic layer was dried (MgSO4) and concentrated. The residue was purified (FCC) to give imidazo[1,2-b]pyridazin-3-yl-carbamic acid phenyl ester (285 mg, 72%). MS (ESI+): calcd for C13H10N4O2 m/z 254.08, found 255.3 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598356B2
Source datasetuspto-grants-2013_12
ORD IDord-1cada48fa53a4ab0bc24f7868c7b5391
Source noteuspto-grants-2013_12