HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 730756Erstellt: 25. Oktober 2026
Diisopropylethylamine → HCID 178461512, Verbindung
https://huagongshe.com/reaction/730756
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | 2-Methylpiperazine, (R)- | HCID 7330434 | — |
| Edukt | 1H-Benzimidazole, 2,7-dichloro-5-(trifluoromethyl)- | HCID 66937336 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Produkt | HCID 178461512 | HCID 178461512 | — |
Reaktionsschritte
A mixture of 2,4-dichloro-6-trifluoromethyl-1H-benzoimidazole (0.51 g, 2 mmol, Example 5b), (R)-(−)-2-methylpiperazine (0.25 g. 2.5 mmol) and N,N-diisopropylethylamine (0.5 mL, 2.9 mmol) in NMP (5 mL) was heated at 120° C. for 16 h. The reaction mixture was cooled to room temperature, diluted with water (10 mL) and extracted with EtOAc (2×20 mL). The combined organic phases were washed with brine (10 mL), dried over Na2SO4 and filtered. The filtrate was concentrated in vacuo and the residue was purified by silica gel chromatography, eluting with 10% MeOH in dichloromethane to give the title compound as a light-yellow solid. MS (ESI, pos. ion) m/z: 319 (M+1).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07582761B2 |
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| Quelldatensatz | uspto-grants-2009_09 |
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| ORD ID | ord-89b01c30d9f344f7a4ca34bf0698a701 |
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| Quellennotiz | uspto-grants-2009_09 |
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