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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 250408Erstellt: 26. Oktober 2026

Water → 1-Bromo-4-hydroxy-isoquinoline-3-carboxylic acid butyl ester

https://huagongshe.com/reaction/250408

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktPhosphorus oxybromideHCID 24613—
Edukt1,4-Dihydroxy-isoquinoline-3-carboxylic acid butyl esterHCID 178450843—
LösungsmittelAcetonitrileHCID 6342—
Produkt1-Bromo-4-hydroxy-isoquinoline-3-carboxylic acid butyl esterHCID 860145413,9%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

2 g (7.7 mmol) of 1,4-Dihydroxy-isoquinoline-3-carboxylic acid butyl ester (from Example D-20 b) dissolved in 100 ml of acetonitrile. 15.4 g (53.6 mmol) of phosphorous oxybromide added to solution and mixture stirred at 80° C. for 64 h. 100 ml of water was added to mixture, and mixture was removed from heat. Mixture was partitioned between ethyl acetate and water. Two phases were separated and the aqueous layer was extracted with ethyl acetate. Organic layers were combined, washed with brine, dried over magnesium sulfate, filtered, and evaporated. Residue was purified by silica gel flash chromatography to give 0.1 g (0.3 mmol) of product. 1H NMR (200 MHz, CDCl3) δ 11.89 (s, 1H), 8.41 (m, 1H), 8.25 (m, 1H), 7.84 (m, 2H), 4.49 (t, J=7.0 Hz, 2H), 1.87 (m, 2H), 1.47 (m, 2H), 1.00 (t, J=7.2 Hz, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07863292B2
Quelldatensatzuspto-grants-2011_01
ORD IDord-10cff72e97344bb4b8e20239bd6c170d
Quellennotizuspto-grants-2011_01