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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tributylamine | HCID 7622 | — |
| Reactant | N,N-Bis(2-chloroethyl)benzenesulfonamide | HCID 315320 | — |
| Reactant | Methyl 5-aminobenzofuran-2-carboxylate | HCID 10845388 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 5[4-(benzenesulfonyl)-1-piperazinyl]benzofuran-2-carboxylate | HCID 90022245 | 53.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09315456B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-a77bf8e7dd2940d791f48c8e11edb982 |
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| Source note | uspto-grants-2016_04 |
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