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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 331115Generated: October 27, 2026

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

https://huagongshe.com/reaction/331115

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 numberUS08877769B2
Source datasetuspto-grants-2014_11
ORD IDord-fb265ad5553948099f0e42a99bed7eb3
Source noteuspto-grants-2014_11