HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
cis-3-Chloroacrylic acid → HCID 178520646, Verbindung
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | cis-3-Chloroacrylic acid | HCID 643794 | — |
| Edukt | HCID 178447227 | HCID 178447227 | — |
| Edukt | HCID 178460972 | HCID 178460972 | — |
| Produkt | HCID 178520646 | HCID 178520646 | — |
Reaktionsschritte
Following the acetylation and desilylation procedure employed for the preparation of (2E)-N-[2-hydroxy-4-({[(Z)-(6-iodo-1,3-dioxo-2,3-dihydroisoquinolin-4(1H)-ylidene)methyl]amino}methyl)phenyl]-2-methylbut-2-enamide, (4Z)-4-[({4-amino-3-[(triisopropylsilyl)oxy]benzyl}amino)methylene]-6-iodoisoquinoline-1,3(2H,4H)-dione (65 mg, 0.11 mmol) is reacted with acid chloride derived from cis-3-chloroacrylic acid (0.12 g, 1.1 mmol). Following desilylation and precipitation, (2Z)-3-chloro-N-[2-hydroxy-4-({[(Z)-(6-iodo-1,3-dioxo-2,3-dihydroisoquinolin-4(1H)-ylidene)methyl]amino}methyl)phenyl]acrylamide is obtained as a solid (10 mg, 17
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07713994B2 |
| Quelldatensatz | uspto-grants-2010_05 |
| ORD ID | ord-ded8a8a9405a4fad95583118affcb622 |
| Quellennotiz | uspto-grants-2010_05 |