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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 370271Erstellt: 23. Oktober 2026

Xanthene-9-carboxylic acid → N-[9-(cyclooctylmethyl)-9-azabicyclo[3.3.1]nonan-3-yl]xanthene-9-carboxamide

https://huagongshe.com/de/reaction/370271

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktXanthene-9-carboxylic acidHCID 65736—
Edukt1-HydroxybenzotriazoleHCID 75771—
Edukt1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
EduktTert-butyl 3-amino-9-azabicyclo[3.3.1]nonane-9-carboxylateHCID 23283006—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
ProduktN-[9-(cyclooctylmethyl)-9-azabicyclo[3.3.1]nonan-3-yl]xanthene-9-carboxamideHCID 1548066992,9%

Reaktionsschritte

15 ml of anhydrous N,N-dimethylformamide suspension having 165 mg of 3-amino-9-t-butoxycarbonyl-9-azabicyclo[3.3.1]nonane and 155 mg of xanthene-9-carboxylic acid was cooled with ice, and 224 mg of EDCI.HCl and 157 mg of 1-hydroxybenzotriazole were successively added thereto. The temperature was raised to room temperature immediately, and the reaction mixture was stirred for 21 hours. 10 ml of water was added to the reaction solution, followed by extraction with diethyl ether. The organic layer was washed with 10% citric acid solution, saturated aqueous sodium bicarbonate, water and saturated aqueous sodium chloride, followed by drying over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and 301 mg of the title compound as a white solid was obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06140338
Quelldatensatzuspto-grants-2000_10
ORD IDord-37a5a51b4e0a4336a8ee8e83cf8c5826
Quellennotizuspto-grants-2000_10