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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507805Generated: October 25, 2026

Acetic Anhydride → Furo(3,4-b)pyrazine-5,7-dione

https://huagongshe.com/reaction/507805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant2,3-Pyrazinedicarboxylic acidHCID 66628—
ProductFuro(3,4-b)pyrazine-5,7-dioneHCID 78482—

Reaction Conditions

Temperature115 °C

Reaction Steps

In a clean 500 ml R. B. flask charged pyrazine-2,3-dicaroxylic acid (50 gms) and acetic anhydride (162 gms). The reaction mass was heated to 110-120° C. till the completion of reaction to get pyrazine-2,3-dicarboxylic acid anhydride. After completion of the reaction, excess acetic anhydride was distilled out under vacuum and furthermore charged with methylene dichloride (315 ml) and 2-amino-5-chloropyridine (40 gms) in a lot wise manner at room temperature for 30 min. Further, the reaction mixture was stirred for 2 hours at room temperature. The reaction mass was cooled to 5 to 10° C. for one hour, the product was filtered and washed with chilled methylene dichloride. The solid was charged with methylene dichloride (235 ml), triethylamine (40.9 ml) at a temp. of 0-5° C. followed by ethyl chloroformate (28.1 ml). The reaction mass was stirred at 0-5° C. for 1 hr, water (200 ml) was added to the reaction mixture and the mass stirred at room temperature for 1 hr to obtain the solids. The title compound thus separated was isolated by filtration.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786304B2
Source datasetuspto-grants-2010_08
ORD IDord-772cf84ff08f43d8b9d1780a47aedf91
Source noteuspto-grants-2010_08