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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1398572Erstellt: 26. Oktober 2026

Morpholine → 6-bromo-3-[(morpholin-4-yl)carbonyl]-1H-indazole

https://huagongshe.com/reaction/1398572

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMorpholineHCID 8083—
Edukt1,1'-CarbonyldiimidazoleHCID 68263—
Edukt6-Bromo-1H-indazole-3-carboxylic acidHCID 24728028—
LösungsmittelDimethylformamideHCID 6228—
Produkt6-bromo-3-[(morpholin-4-yl)carbonyl]-1H-indazoleHCID 68181854—

Reaktionsbedingungen

Temperatur45 °C

Reaktionsschritte

To a solution of 6-bromo-1H-indazole-3-carboxylic acid (500 mg, 2.07 mmol) in DMF (10 mL) was added CDI (403.62 mg, 2.49 mmol) and the reaction mixture stirred at 45° C. for 40 minutes. Morpholine (0.36 ml, 4.16 mmol) was then added and the reaction mixture stirred at RT. The reaction mixture was quenched by diluting with water. The product was extracted into EtOAc (×2) and the combined organic extracts were then washed with water and brine and dried (Na2SO4), filtered and concentrated in vacuo to give the crude (78% pure) title compound: 1H NMR (500 MHz, DMSO) delta 3.58-3.79 (6H, m), 3.96-4.13 (2H, m), 7.36 (1H, dd, J=8.59, 1.66 Hz), 7.86 (1H, d, J=1.10 Hz), 7.93 (1H, s), 13.66 (1H, br. s.); LC-MS: m/z=+311.70 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08901313B2
Quelldatensatzuspto-grants-2014_12
ORD IDord-6a77fbb8c287432299f1dcd7d3ba975a
Quellennotizuspto-grants-2014_12