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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 628793Generated: October 29, 2026

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

https://huagongshe.com/reaction/628793

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

Temperature75 °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 stifling 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 numberUS09315456B2
Source datasetuspto-grants-2016_04
ORD IDord-a77bf8e7dd2940d791f48c8e11edb982
Source noteuspto-grants-2016_04