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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 40035Erstellt: 24. Oktober 2026

Boron tribromide → 1-Benzyl-N-(3,4-difluorobenzyl)-6-hydroxy-2-isopropyl-1H-indole-3-carboxamide

https://huagongshe.com/de/reaction/40035

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBoron tribromideHCID 25134—
Edukt1-Benzyl-N-(3,4-difluorobenzyl)-2-isopropyl-6-methoxy-1H-indole-3-carboxamideHCID 44159276—
LösungsmittelDichloromethaneHCID 6344—
Produkt1-Benzyl-N-(3,4-difluorobenzyl)-6-hydroxy-2-isopropyl-1H-indole-3-carboxamideHCID 25160740—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of 1-benzyl-N-(3,4-difluorobenzyl)-2-isopropyl-6-methoxy-1H-indole-3-carboxamide (Compound 7, 452 mg, 1.0 mmol) in CH2Cl2 (20 ml) at 0° C. was added BBr3 (1.0 M in CH2Cl2, 3.0 ml, 3.0 mmol) dropwise. The reaction was stirred for 1 h at 0° C. and 1 h at room temperature, quenched with ice, extracted with EtOAc, the organic layer was washed with brine, dried over Na2SO4, and concentrated in vacuo. The residue was purified by chromatography on silica gel (0→50% EtOAc-hexanes) to yield the title compound as a yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08524917B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-25f4e497f4f04357950d61bfc102aa0e
Quellennotizuspto-grants-2013_09