HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 456422Erstellt: 25. Oktober 2026
Diisopropylethylamine → (R)-2-[6-(4-Trifluoromethyl-phenyl)-pyridazin-3-yl]-octahydro-pyrido[1,2-a]pyrazine
https://huagongshe.com/reaction/456422
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | Tetrafluoro-m-phenylenediamine dihydrochloride | HCID 149026 | — |
| Edukt | (R)-Octahydro-pyrido[1,2-a]pyrazine | HCID 773775 | — |
| Edukt | Pyridazine, 3-chloro-6-[4-(trifluoromethyl)phenyl]- | HCID 12449554 | — |
| Lösungsmittel | Dimethyl Sulfoxide | HCID 679 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | (R)-2-[6-(4-Trifluoromethyl-phenyl)-pyridazin-3-yl]-octahydro-pyrido[1,2-a]pyrazine | HCID 20799063 | 98,1% |
Reaktionsschritte
A mixture of the dihydrochloride salt of (R)-octahydropyrido[1,2-a]pyrazine (649 mg, 3.05 mmol), diisopropylethylamine (1.17 ml, 6.72 mmol), 3-chloro-6-(4-trifluoromethylphenyl)-pyridazine (290 mg, 1.12 mmol) and dimethylsulfoxide (1 ml) was heated in a closed vessel at 160° C. for 40 min. The reaction mixture was cooled to room temperature, diluted with dichloromethane (10 ml) and washed with water (2×15 ml) and brine (15 ml). The organic layer was dried over magnesium sulphate. The solvent was removed in vacuo to give 398 mg of the title compound as the free base.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07186721B2 |
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| Quelldatensatz | uspto-grants-2007_03 |
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| ORD ID | ord-bfd189a0842d47fd8b77df7eb5d727b1 |
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| Quellennotiz | uspto-grants-2007_03 |
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