HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 418316Erstellt: 24. Oktober 2026
Hydrochloric Acid → 5-Methyl-3-phenylisoxazole-4-carboxylic acid [4-dimethylamino-4-(3-fluorophenyl)cyclohexyl]amide hydrochloride
https://huagongshe.com/de/reaction/418316
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Chlorotrimethylsilane | HCID 6397 | — |
| Edukt | 5-Methyl-3-phenylisoxazole-4-carboxylic acid | HCID 14343 | — |
| Edukt | 1-(3-fluorophenyl)-N,N-dimethylcyclohexane-1,4-diamine | HCID 57904199 | — |
| Edukt | 5-Methyl-3-phenylisoxazole-4-carboxylic acid [4-dimethylamino-4-(3-fluorophenyl)cyclohexyl]amide | HCID 66651535 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Lösungsmittel | Methyl Ethyl Ketone | HCID 6569 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Lösungsmittel | Diethyl ether methanol | HCID 21864698 | — |
| Produkt | 5-Methyl-3-phenylisoxazole-4-carboxylic acid [4-dimethylamino-4-(3-fluorophenyl)cyclohexyl]amide hydrochloride | HCID 66651639 | — |
Reaktionsschritte
As described for Example 120, 700 mg of a cis-trans mixture of 1-(3-fluorophenyl)-N,N-dimethylcyclohexane-1,4-diamine were reacted with 600 mg 5-methyl-3-phenylisoxazole-4-carboxylic acid (1 molar equivalent) and the crude product was isolated. The main fraction, obtained after column chromatography on silica gel (3.0×19 cm) with 175 ml diethyl ether followed by 250 ml diethyl ether/methanol (V:V=2:1), 250 ml diethyl ether/methanol (V:V=1:1) and 200 ml methanol, of 775 mg was dissolved in 10 ml 2-butanone and 10 ml ethyl acetate and converted into the corresponding hydrochloride of the non-polar diastereoisomer of 5-methyl-3-phenylisoxazole-4-carboxylic acid [4-dimethylamino-4-(3-fluorophenyl)cyclohexyl]amide by adding 33 μl water and 233 μl chlorotrimethylsilane (423 mg of white solid, Mp. 256-259° C.).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08093272B2 |
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| Quelldatensatz | uspto-grants-2012_01 |
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| ORD ID | ord-e8b5abc0164a451394ad1fff15b0e26c |
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| Quellennotiz | uspto-grants-2012_01 |
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