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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 628796Generated: October 26, 2026

Ammonia → 5-(Piperazin-1-yl)benzofuran-2-carboxamide

https://huagongshe.com/reaction/628796

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantHydrochloric AcidHCID 313—
ReactantMethyl 5-(piperazin-1-yl)benzofuran-2-carboxylateHCID 77231352—
SolventWaterHCID 962—
Product5-(Piperazin-1-yl)benzofuran-2-carboxamideHCID 983471973.1%

Reaction Steps

Methyl 5-(1-piperazinyl)benzofuran-2-carboxylate (37 g) was added to saturated methanolic ammonia solution (1850 ml) at 25-30° C., the mixture was stirred for 6 to 16 hours at the same temperature. The reaction mass was distilled under vacuum to remove the solvent after completion of the reaction. Water (148 ml) was added to the resulting residue, followed by adjusting the pH to 2-4 with concentrated HCl and then filtering the aqueous layer. The pH of the resulting aqueous layer was adjusted to 9-10 with ammonium hydroxide solution. The separated solid was filtered, washed with water (100 ml) and then dried to produce 25.5 g of 5-(1-piperazinyl)benzofuran-2-carboxamide (Purity by HPLC: 99%; Yield: 73.1%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315456B2
Source datasetuspto-grants-2016_04
ORD IDord-6cf50d02d20e40c0b6bc0d3da7cd02ad
Source noteuspto-grants-2016_04