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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1173108Erstellt: 26. Oktober 2026

Ammonia → 1H-pyrrolo[2,3-c]pyridin-7-amine

https://huagongshe.com/reaction/1173108

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmoniaHCID 222—
Edukt2-Bromo-3-nitropyridineHCID 555054—
Edukt7-Bromo-6-azaindoleHCID 19696456—
KatalysatorCopperHCID 23978—
Produkt1H-pyrrolo[2,3-c]pyridin-7-amineHCID 19080186—

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

To 84 ml of aqueous concentrated ammonia were added 600 mg (3.05 mmol) of 7-bromo-1H-pyrrolo[2,3-c]pyridine synthesized from 2-bromo-3-nitropyridine in the same manner as in Production Example 1a, 194 mg of a copper powder and 603 mg of cuprous chloride. The mixture was heated in a sealed tube at 120° C. for 15 hours and then treated, to give 170 mg of 7-amino-1H-pyrrolo[2,3-c]pyridine. The resulting product was reacted and treated in the same manner as in Examples 1a and 2a, to give 57 mg of the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07834049B2
Quelldatensatzuspto-grants-2010_11
ORD IDord-1984b068d707462f827e7c0a08a19cc2
Quellennotizuspto-grants-2010_11