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1H-Pyrrolo[2,3-b]pyridine-3-carboxamide(9CI) synthesis

3synthesis methods
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Yield:74420-16-9 95%

Reaction Conditions:

Stage #1: 1H-pyrrolo[2,3-b]pyridine-3-carbonitrilewith sulfuric acid at 20; for 1 h;
Stage #2: with sodium hydroxide

Steps:

3.1.3. General Procedure for the Synthesis of 1H-Pyrrolo[2,3-b]pyridine-3-carboxamides (6a,b)

General procedure: A solution of appropriate carbonitriles 5a,b (6.3 mmol) in concentrate sulphuric acid (3.32 mL) was stirred at room temperature for 15-60 min. The solution was slowly poured into ice and basified with concentrated NaOH. The residue was extracted with ethyl acetate (3 × 20 mL), dried (Na2SO4) and concentrated under reduced pressure to afford the carboxamides 6a,b.

References:

Carbone, Anna;Parrino, Barbara;Vita, Gloria Di;Attanzio, Alessandro;Span, Virginia;Montalbano, Alessandra;Barraja, Paola;Tesoriere, Luisa;Livrea, Maria Antonia;Diana, Patrizia;Cirrincione, Girolamo [Marine Drugs,2015,vol. 13,# 1,p. 460 - 492]