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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 402815Erstellt: 25. Oktober 2026

6-Methoxy-1H-indole-3-carboxaldehyde → 1-cyclopropyl-6-methoxy-1H-indole-3-carbaldehyde

https://huagongshe.com/reaction/402815

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt6-Methoxy-1H-indole-3-carboxaldehydeHCID 907214—
EduktCyclopropylboronic acidHCID 2760897—
LösungsmittelDichloromethaneHCID 6344—
Produkt1-cyclopropyl-6-methoxy-1H-indole-3-carbaldehydeHCID 8668527140,9%

Reaktionsschritte

Dihydroxo-bis[N,N,N′,N′-tetramethylenediamine)copper (II) chloride (26 mg, 0.057 mmol) was added to a stirred room temperature mixture of 6-methoxy-1H-indole-3-carbaldehyde (100 mg, 0.568 mmol) and cyclopropylboronic acid (98 mg, 1.13 mmol) in dichloromethane (3 mL). Molecular sieves (4 A°, 100 mg) were added and the mixture was stirred under oxygen at room temperature for 48 hours. The reaction mixture was filtered over a pad of silica gel, washed with dichloromethane, partitioned between dichloromethane (10 mL) and 10% ammonium hydroxide (2×10 mL). The organic layer was washed with water (10 mL) and brine (10 mL). The organic layer was dried over sodium sulfate, filtered and concentrated under reduced pressure. The residue was purified by flash chromatography (Biotage 25 M), eluting with EtOAc/hexanes to give the title compound (50 mg) as a oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08742110B2
Quelldatensatzuspto-grants-2014_06
ORD IDord-bd40677a9d6c4dbc9e8ae4271c401b3c
Quellennotizuspto-grants-2014_06