HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Water → N-1,2-Benzisoxazol-3-yl-4-(3-isopropyl-1,2,4-thiadiazol-5-yl)piperazine-1-carboxamide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 5-Chloro-3-(propan-2-yl)-1,2,4-thiadiazole | HCID 12874683 | — |
| Edukt | N-1,2-Benzisoxazol-3-ylpiperazine-1-carboxamide trifluoroacetate | HCID 68778018 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | N-1,2-Benzisoxazol-3-yl-4-(3-isopropyl-1,2,4-thiadiazol-5-yl)piperazine-1-carboxamide | HCID 68782168 | 20,3% |
Reaktionsschritte
To a solution of 5-chloro-3-isopropyl-1,2,4-thiadiazole (90.3 mg, 0.555 mmol) and N-1,2-benzisoxazol-3-ylpiperazine-1-carboxamide trifluoroacetate (200 mg, 0.555 mmol) in N,N-dimethylformamide (2 ml) was added triethylamine (0.389 ml, 2.78 mmol) at room temperature, and the mixture was stirred at room temperature for 2 hours. The reaction mixture was poured to water, and the precipitated solid was separated by filtration, which was recrystallized from a mixed solvent of ethyl acetate and tetrahydrofuran to give 42.0 mg (20.3%) of the desired product. mp 178-179° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07851473B2 |
| Quelldatensatz | uspto-grants-2010_12 |
| ORD ID | ord-55e6b39fa5f7449ab40a57f5ce0dedc2 |
| Quellennotiz | uspto-grants-2010_12 |