HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1049126Erstellt: 25. Oktober 2026
Diisopropylethylamine → 5-chloro-N-[(1S)-2,2,2-trifluoro-1-methylethyl]pyrazine-2-carboxamide
https://huagongshe.com/reaction/1049126
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | 5-Chloropyrazinoic acid | HCID 465472 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Edukt | (S)-1,1,1-trifluoropropan-2-amine | HCID 10964447 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 5-chloro-N-[(1S)-2,2,2-trifluoro-1-methylethyl]pyrazine-2-carboxamide | HCID 86675754 | 74,1% |
Reaktionsschritte
N,N-Diisopropylethylamine (1.3 mL, 7.5 mmol) was added to a mixture of 5-chloropyrazine-2-carboxylic acid (0.40 g, 2.5 mmol), N,N,N′,N′-tetramethyl-O-(7-azabenzotriazol-1-yl)uronium hexafluorophosphate (1.0 g, 2.8 mmol) and (2S)-1,1,1-trifluoropropan-2-amine (0.28 g, 2.5 mmol) in methylene chloride (10 mL). The reaction mixture was stirred at room temperature overnight. The reaction mixture was worked up with sat. aqueous NaHCO3, and extracted with ethyl acetate. The combined organic layers were washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure. The residue was purified by flash chromatography on a silica gel column with ethyl acetate in hexanes (0-15%) to afford the desired product (0.47 g, 73%). LCMS cacld. for C8H8ClF3N3O (M+1)+: m/z=254.0. Found: 253.9.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09382231B2 |
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| Quelldatensatz | uspto-grants-2016_07 |
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| ORD ID | ord-a81f90242b474ac394ff16aa1b8441bf |
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| Quellennotiz | uspto-grants-2016_07 |
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