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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1056545Generated: October 31, 2026

Tributylamine → Methyl 5[4-(benzenesulfonyl)-1-piperazinyl]benzofuran-2-carboxylate

https://huagongshe.com/reaction/1056545

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylamineHCID 7622—
ReactantN,N-Bis(2-chloroethyl)benzenesulfonamideHCID 315320—
ReactantMethyl 5-aminobenzofuran-2-carboxylateHCID 10845388—
SolventMethanolHCID 887—
ProductMethyl 5[4-(benzenesulfonyl)-1-piperazinyl]benzofuran-2-carboxylateHCID 9002224553.6%

Reaction Conditions

Temperature27.5 °C

Reaction Steps

Methyl 5-aminobenzofuran-2-carboxylate (200 g) and N-benzenesulfonyl-N,N-bis(2-chloroethyl)amine (289 g) were added to tributyl amine (1012 ml) under stirring at 25-30° C. The resulting mixture was heated to 73-77° C., followed by stirring for 43 hours at the same temperature. The reaction mass was cooled to 25-30° C., followed by the addition of methanol (506 ml) and then stirring for 30 minutes at 25-30° C. The resulting mass was filtered, washed with chilled methanol (200 ml) and then dried to produce 220 g of methyl 5-[4-(benzenesulfonyl)-1-piperazinyl]benzofuran-2-carboxylate as a fine powder (Purity by HPLC: 99.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09399630B2
Source datasetuspto-grants-2016_07
ORD IDord-7ad84633a7d444dca686dfbff2a86a93
Source noteuspto-grants-2016_07