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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 25527Erstellt: 23. Oktober 2026

3-Nitrobenzaldehyde → [5-(5,6-Difluoro-1H-indol-2-yl)-2-methoxy-phenyl]-(3-nitrobenzyl)-amine

https://huagongshe.com/de/reaction/25527

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-NitrobenzaldehydeHCID 7449—
EduktSodium BicarbonateHCID 516892—
EduktSodium triacetoxyborohydrideHCID 5049666—
Edukt5-(5,6-difluoro1H-indol-2-yl)-2-methoxy-phenylamineHCID 9943439—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelDichloromethaneHCID 6344—
Produkt[5-(5,6-Difluoro-1H-indol-2-yl)-2-methoxy-phenyl]-(3-nitrobenzyl)-amineHCID 1011215526,9%

Reaktionsschritte

3-Nitrobenzaldehyde (0.3 g, 2.0 mmol) was added to a stirred mixture of 5-(5,6-difluoro-1H-indol-2-yl)-2-methoxy-phenylamine (0.548 g, 2.0 mmol) in methylene chloride (125 mL), followed by acetic acid (0.2 g). The resulting mixture is stirred at room temperature for 1 hour. Sodium triacetoxyborohydride (0.46 g, 2.2 mmol) was added in one portion, and the resulting homogeneous solution was stirred at room temperature for 6 days. Saturated aqueous sodium bicarbonate solution (100 mL) was added and the mixture was sired for 2 hours. The mixture was shaken, the organic layer was separated and dried over Na2SO4. The solvent was evaporated to give a yellow solid. Recrystallization from methanol gave the product (220 mg), mp 212-214° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06858739B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-cc25dad197fc4974b9fe077fbac97fd9
Quellennotizuspto-grants-2005_02