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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1056548Generated: October 26, 2026

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

https://huagongshe.com/reaction/1056548

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 numberUS09399630B2
Source datasetuspto-grants-2016_07
ORD IDord-c16dad9cfd714f6abcc66ba4f2029e7f
Source noteuspto-grants-2016_07