HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 601304Erstellt: 24. Oktober 2026
Cyclopropanecarboxaldehyde → 3-[7-(benzyloxy)-1,1-dioxido-4H-1,2,4-benzothiadiazin-3-yl]-1-{[cyclopropylmethylene]amino}-4-hydroxyquinolin-2(1H)-one
https://huagongshe.com/de/reaction/601304
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Cyclopropanecarboxaldehyde | HCID 123114 | — |
| Edukt | 1-amino-3-[7-(benzyloxy)-1,1-dioxido-4H-1,2,4-benzothiadiazin-3-yl]-4-hydroxyquinolin-2(1H)-one | HCID 136358484 | — |
| Lösungsmittel | Dimethylacetamide | HCID 31374 | — |
| Produkt | 3-[7-(benzyloxy)-1,1-dioxido-4H-1,2,4-benzothiadiazin-3-yl]-1-{[cyclopropylmethylene]amino}-4-hydroxyquinolin-2(1H)-one | HCID 136358486 | 84,3% |
Reaktionsschritte
The product of Example 304F (0.800 g, 1.73 mmol) and cyclopropane carboxaldehyde (1.60 mL, 20.76 mmol) in N,N-dimethylacetamide (2 mL) were reacted at 120° C. for 60 minutes in a microwave reactor in a sealed tube. The reaction was concentrated under a stream of nitrogen warmed through a manifold heated to 165° C. The resulting residue was triturated with diethyl ether and filtered to give the title compound (0.750 g, 84%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07902203B2 |
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| Quelldatensatz | uspto-grants-2011_03 |
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| ORD ID | ord-1e6e3c471fbc4839a7a09428abf1008f |
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| Quellennotiz | uspto-grants-2011_03 |
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