HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 44402Erstellt: 25. Oktober 2026
4-Methoxybenzylamine → 4-Amino-2-oxo-1,2-dihydroquinoline-3-carbonitrile
https://huagongshe.com/reaction/44402
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 4-Methoxybenzylamine | HCID 75452 | — |
| Edukt | 4-Chloro-1,2-dihydro-2-oxoquinoline-3-carbonitrile | HCID 2777510 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 4-Amino-2-oxo-1,2-dihydroquinoline-3-carbonitrile | HCID 5200312 | 25,1% |
Reaktionsschritte
4-chloro-2-oxo-1,2-dihydroquinoline-3-carbonitrile (example 72) (0.66 g, 3.23 mmol) was suspended in DMF (7 mL), and 4-methoxybenzylamine (0.94 mL, 7.26 mmol) was added. The reaction was heated at 100° C. for 1 hour and the DMF was removed under vacuum. The residue was dissolved in TFA (6 mL) and stirred at room temperature for 30 minutes and dichloromethane (10 mL) was added. The solid product that formed was collected, suspended in water and the solution stirred overnight. The solid was collected by filtration to give 4-amino-2-oxo-1,2-dihydroquinoline-3-carbonitrile (0.150 g, 25%) as a white solid. M.p.: >250° C. 1H NMR (400 MHz, DMSO-d6) δ7.19 (m, 2H), 7.57 (m, 1H), 7.88 (bs, 2H), 8.12 (d, J=7.6 Hz, 1H), 11.23 (s, 1H). MS 186 (MH+).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08541421B2 |
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| Quelldatensatz | uspto-grants-2013_09 |
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| ORD ID | ord-cce9922a5f3b470095ed458999a01420 |
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| Quellennotiz | uspto-grants-2013_09 |
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