HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1676909Erstellt: 24. Oktober 2026
Bumetanide → N,N-diethylaminocarbonylmethyl 3-aminosulfonyl-5-butylamino-4-phenoxybenzoate
https://huagongshe.com/de/reaction/1676909
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Bumetanide | HCID 2471 | — |
| Edukt | Sodium Iodide | HCID 5238 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Chloro-N,N-diethylacetamide | HCID 16844 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | N,N-diethylaminocarbonylmethyl 3-aminosulfonyl-5-butylamino-4-phenoxybenzoate | HCID 16657241 | 63,6% |
Reaktionsschritte
Bumetanide (1.2 g, 3.29 mmol) was dissolved in dimethylformamide (12 mL) and 2-chloro-N,N-diethylacetamide (500 mg, 3.35 mmol) was added followed by triethylamine (0.68 mL) and sodium iodide (500 mg 3.33 mmol). The reaction was heated to 95° C. for 8 hours, at which time TLC and LC/MS indicated the reaction was complete. The reaction was cooled to room temperature brought up in dichloromethane and washed with water, saturated ammonium chloride and reduced to a thick slurry. To the slurry was added water (25 mL), and the resultant solids precipitated from the solution. The product was filtered and dried in a vacuum oven at 50° C. for 12 hours to yield 1.0 g of N,N-diethylaminocarbonylmethyl 3-aminosulfonyl-5-butylamino-4-phenoxybenzoate.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08008283B2 |
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| Quelldatensatz | uspto-grants-2011_08 |
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| ORD ID | ord-57c9f7a2ffad4d7c8419fcd840a53bf9 |
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| Quellennotiz | uspto-grants-2011_08 |
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