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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253589Generated: October 26, 2026

Ammonium formate → 2-(4-fluorophenyl)-6-(hexahydropyrrolo[3,4-c]pyrrol-2-(1H)-yl)-3-(pyridazin-4-yl)-imidazo[1,2-b]pyridazine

https://huagongshe.com/reaction/1253589

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
Reactant6-(5-benzylhexahydropyrrolo[3,4-c]pyrrol-2-(1H)-yl)-2-(4-fluorophenyl)-3-(pyridazin-4-yl)-imidazo[1,2-b]pyridazineHCID 25204667—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product2-(4-fluorophenyl)-6-(hexahydropyrrolo[3,4-c]pyrrol-2-(1H)-yl)-3-(pyridazin-4-yl)-imidazo[1,2-b]pyridazineHCID 25226802—

Reaction Steps

The mixture of 1.2 g (2.4 mmol) of 6-(5-benzylhexahydropyrrolo[3,4-c]pyrrol-2-(1H)-yl)-2-(4-fluorophenyl)-3-(pyridazin-4-yl)-imidazo[1,2-b]pyridazine and 2.3 g (36 mmol) of ammonium formate in 40 ml of methanol is refluxed for 2 hours in the presence of palladium-on-charcoal (10%) containing 50% moisture.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455491B2
Source datasetuspto-grants-2013_06
ORD IDord-19c22ecc74bd452384763aa6dc5f215c
Source noteuspto-grants-2013_06