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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1958324Generated: October 25, 2026

Furo(3,4-b)pyrazine-5,7-dione → 3-(2-Phenyl-imidazo[1,2-a]pyrimidin-7-ylcarbamoyl)-pyrazine-2-carboxylic acid

https://huagongshe.com/reaction/1958324

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFuro(3,4-b)pyrazine-5,7-dioneHCID 78482—
Reactant2-Phenylimidazo[1,2-A]pyrimidin-7-amineHCID 50878390—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDimethylformamideHCID 6228—
Product3-(2-Phenyl-imidazo[1,2-a]pyrimidin-7-ylcarbamoyl)-pyrazine-2-carboxylic acidHCID 6738776947%

Reaction Conditions

Temperature78 °C

Reaction Steps

Furo[3,4-b]pyrazine-5,7-dione (736 mg, 4.9 mmol) and DMAP (58 mg, cat.) were added to a solution of 2-phenyl-imidazo[1,2-a]pyrimidin-7-ylamine (example 1, step 1, 1.00 g, 4.8 mmol) in DMF (25 ml). The mixture was heated to 78° C. overnight, and cooled to RT. The formed precipitate was collected by filtration, and residual solvent was removed under vacuum. The thus obtained crude product (800 mg, 47%) was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410117B2
Source datasetuspto-grants-2013_04
ORD IDord-8d4635bc6bb74226ba7ef648f8d31a82
Source noteuspto-grants-2013_04