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HRID 1820891Erstellt: 27. Oktober 2026

N,N-Diethyl-2-propanamine → [3-(3,4-Dimethoxy-phenyl)-pyrrolo[2,3-b]pyridin-1-yl]-(2-ethoxy-4-nitro-phenyl)-methanone

https://huagongshe.com/reaction/1820891

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN,N-Diethyl-2-propanamineHCID 521913—
EduktPyBroPHCID 2733179—
Edukt2-Ethoxy-4-nitrobenzoic acidHCID 2736347—
Edukt3-(3,4-dimethoxy-phenyl)-1H-pyrrolo[2,3-b]pyridineHCID 11673285—
LösungsmittelDichloromethaneHCID 6344—
Produkt[3-(3,4-Dimethoxy-phenyl)-pyrrolo[2,3-b]pyridin-1-yl]-(2-ethoxy-4-nitro-phenyl)-methanoneHCID 5789170277,5%

Reaktionsschritte

3-(3,4-Dimethoxy-phenyl)-1H-pyrrolo[2,3-b]pyridine 1(250 mg, 0.98 mmole) was dissolved in 50 mL of CH2Cl2. N,N-diethylisopropylamine (205 uL, 1.2 mmol), 2-ethoxy-4-nitro-benzoic acid (228 mg, 1.1 mmol) and bromotris(pyrolodino)phoshonium hexafluorophosphate (550 mg, 1.1 mmol) were added to the stirring reaction mixture. The mixture was stirred at ambient temperature for 4 h and washed consecutively with saturated sodium bicarbonate and saturated potassium bisulfate solution. The resulting solution was dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was purified by silica gel chromatography (30% ethyl acetate in hexanes) to yield 340 mg (77%) of the titled compound as a yellow solid. MS(ESI) [M+H+]+=448.2.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07605168B2
Quelldatensatzuspto-grants-2009_10
ORD IDord-3a8ccfd22a4e4c6b98e6fdbdda52c2a2
Quellennotizuspto-grants-2009_10