Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 2-Methyl-2-butanol | HCID 6405 | — |
| Edukt | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 8-Fluoro-4-methoxy-2,5-dimethylthiochroman-6-carboxylic acid-1,1-dioxide | HCID 15278521 | — |
| Edukt | HCID 178418331 | HCID 178418331 | — |
| Produkt | HCID 178463135 | HCID 178463135 | 76,8% |
Reaktionsschritte
In a 50-ml flask, 0.70 g (0.0023 mol) of 8-fluoro-4-methoxy-2,5-dimethylthiochroman-6-carboxylic acid-1,1-dioxide, 0.28 g (0.0025 mol) of 1-ethyl-5-hydroxypyrazole and 0.52 g (0. 0025 mol) of DCC (N,N'-dicyclohexylcarbodiimide) were added to 5 ml of tert-amyl alcohol at the same time, and the mixture was stirred at room temperature for 30 minutes. Then, 0.17 g (0.00125 mol) of anhydrous potassium carbonate was added. The reaction mixture was allowed to react at 80° C. for 8 hours, and then the reaction solvent was distilled off under reduced pressure. The remainder was dispersed in a 2% potassium carbonate aqueous solution and ethyl acetate to separate it into two phases. Further, the aqueous phase was acidified with 5% hydrochloric acid, and the precipitated oil was extracted with ethyl acetate. The extract was dried over anhydrous sodium sulfate and then concentrated under reduced pressure to give 0.70 g of 8-fluoro-4-methoxy-2,5-dimethyl-6-(1-ethyl-5-hydroxypyrazol-4-yl)carbonylthiochroman-1,1-dioxide (Compound 40) shown in Table 5. The yield thereof was 78%.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US05468722 |
|---|
| Quelldatensatz | uspto-grants-1995_11 |
|---|
| ORD ID | ord-4fcb4cdc1c714c79bbfc206f222e3c19 |
|---|
| Quellennotiz | uspto-grants-1995_11 |
|---|