HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Diisopropylamine → S-1-(4-Fluorophenyl)-1H-indazol-5-yl benzothioate
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Diisopropylamine | HCID 7912 | — |
| Edukt | 3,4,7,8-Tetramethyl-1,10-phenanthroline | HCID 74265 | — |
| Edukt | 1-(4-fluorophenyl)-5-iodo-1H-indazole | HCID 59251128 | — |
| Edukt | HCID 178526132 | HCID 178526132 | — |
| Katalysator | HCID 178505377 | HCID 178505377 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | S-1-(4-Fluorophenyl)-1H-indazol-5-yl benzothioate | HCID 59339848 | 20% |
Reaktionsschritte
To a solution of 1-(4-fluorophenyl)-5-iodo-1H-indazole (103e, 0.224 g, 0.66 mmol), thiobenzoic acid (0.093 ml, 0.79 mmol), 3,4,7,8-tetramethyl-1,10-phenantroline (0.031 g, 0.13 mmol) and N,N-diisopropylamine (0.220 ml, 1.32 mmol) in toluene (2.5 ml) was added copper(I) iodine (2.245 μl, 0.07 mmol). The resulting mixture was stirred at 110 C O/N. The reaction mixture was cooled to r.t. diluted with EtOAc and washed with water. The organic phase was the dried the solvent evaporated and then purified on HPLC. The relevant fractions were collected freezdried to give 45 mg of product (20% yield) which was analysed by LC/MS.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07728030B2 |
| Quelldatensatz | uspto-grants-2010_06 |
| ORD ID | ord-5b1dc549e4134f18b2f42ea77cf3f868 |
| Quellennotiz | uspto-grants-2010_06 |