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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 269994Erstellt: 26. Oktober 2026

Pyridine → 7-Phenyl-isoquinoline-5-sulfonic acid (2-amino-ethyl)-amide

https://huagongshe.com/reaction/269994

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktN-BOC-ethylenediamineHCID 187201—
EduktSodium BicarbonateHCID 516892—
Edukt7-BromoisoquinolineHCID 12257441—
EduktHCID 178527254HCID 178527254—
LösungsmittelDichloromethaneHCID 6344—
Produkt7-Phenyl-isoquinoline-5-sulfonic acid (2-amino-ethyl)-amideHCID 1129035650%

Reaktionsbedingungen

Temperatur155 °C

Reaktionsschritte

A mixture of 7-bromoisoquinoline (6.5 g, 31.24 mmol) in HSO3Cl (60 mL) is heated to 155° C. with stirring under N2 overnight, and then cooled to room temperature and slowly poured into ice water. After neutralizing with NaHCO3 at 0° C., sulfonyl chloride is extracted with methylene chloride. The organic layer is dried over Na2SO4 and concentrated to 100 mL and dropped to a solution of N-t-butoxycarbonylethylene diamine (5.01 g, 31.24 mmol) in pyridine (2.54 mL, 31.24 mmol) and CH2Cl2 (120 mL). After stirring overnight, the mixture is concentrated, and the residue is dissolved in EtOAc, which is washed with citric acid solution (50%) and brine. The crude material is purified by chromatography over silica gel (gradient 20% hexane in EtOAc) to give 6.50 g (50% yield) of desired product

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07449477B2
Quelldatensatzuspto-grants-2008_11
ORD IDord-fa0fb79887d646c5b27ca47b1d14f14a
Quellennotizuspto-grants-2008_11