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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1616650Erstellt: 25. Oktober 2026

N-cyclohexyl-N'-(2-morpholinoethyl)-carbodiimide methyl-p-toluenesulfonate → 4-Methoxy-9-aza-tricyclo[6.3.1.0*2,7*]dodeca-2,4,6-trien-10-one

https://huagongshe.com/reaction/1616650

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-cyclohexyl-N'-(2-morpholinoethyl)-carbodiimide methyl-p-toluenesulfonateHCID 9954069—
Edukt3-Carboxymethyl-5-methoxy-indan-1-yl-ammonium chlorideHCID 86656208—
LösungsmittelPyridineHCID 1049—
Produkt4-Methoxy-9-aza-tricyclo[6.3.1.0*2,7*]dodeca-2,4,6-trien-10-oneHCID 66941775—

Reaktionsschritte

3-Carboxymethyl-5-methoxy-indan-1-yl-ammonium chloride (13.2 g) and 1-cyclohexyl-3-(2-morpholinoethyl)carbodiimide methyl-p-toluenesulfonate (21.7 g) dissolved in pyridine (500 mL) are stirred at room temperature for 7 d. Then, the pyridine is removed under reduced pressure and the residue is taken up in water (200 mL) and dichloromethane (200 mL). The organic phase is separated and the aqueous phase is extracted twice with dichloromethane. The combined organic phases are washed with 1 M hydrochloric acid, 1 M NaOH solution, and water. After drying (MgSO4), the solvent is evaporated under reduced pressure to yield the product as a beige solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08765780B2
Quelldatensatzuspto-grants-2014_07
ORD IDord-b96a7ee837fb482a927988a49d3863cb
Quellennotizuspto-grants-2014_07