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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 422014Erstellt: 25. Oktober 2026

Pyrrole-2-carboxaldehyde → 2-Oxo-3-(1h-pyrrol-2-ylmethylene)-2,3-dihydro-1h-indole-6-carboxylic acid (3-benzoylamino-phenyl)-amide

https://huagongshe.com/reaction/422014

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyrrole-2-carboxaldehydeHCID 13854—
Edukt2-oxo-2,3-dihydro-1H-indole-6-carboxylic acid (3-benzoylamino-phenyl)-amideHCID 66675495—
KatalysatorPiperidineHCID 8082—
LösungsmittelEthanolHCID 702—
Produkt2-Oxo-3-(1h-pyrrol-2-ylmethylene)-2,3-dihydro-1h-indole-6-carboxylic acid (3-benzoylamino-phenyl)-amideHCID 66674790—

Reaktionsschritte

To a solution of 2-oxo-2,3-dihydro-1H-indole-6-carboxylic acid (0.20 g, 1.1 mmol) in DMF (1 ml) is added N-(3-amino-phenyl)-benzamide (0.26 g, 1.2 mmol), N,N-diisopropylethylamine (0.44 g, 3.4 mmol) and HATU (0.47 g, 1.24 mmol). The reaction is stirred for 20 hours and concentrated. The residue is purified by HPLC (C18 column, eluted with CH3CN—H2O containing 0.05% TFA) to give 2-oxo-2,3-dihydro-1H-indole-6-carboxylic acid (3-benzoylamino-phenyl)-amide as off-white solid. This amide (15 mg, 0.04 mmol) is then heated with 1H-pyrrole-2-carbaldehyde (6.0 mg, 0.06 mmol) in ethanol (2 ml) in the presence of 2 drops of piperidine at 80° C. for 20 hours. The mixture is concentrated and the desired compound is obtained after HPLC purification: 1H NMR (DMSO-d6) δ 6.41 (s, 1H), 6.93 (s, 1H), 7.31 (t, 1H, J=7.8 Hz), 7.44 (s, 1H), 7.48-7.51 (m, 3H), 7.54 (t, 2H, J=7.2 Hz), 7.59 (d, 1H, J=6.6 Hz), 7.70 (d, 1H, J=8.4 Hz), 7.78 (d, 1H, J=8.4 Hz), 7.92 (s, 1H), 7.98 (d, 2H, J=7.2 Hz), 8.33 (s, 1H), 10.27 (s, 1H), 10.31 (s, 1H), 11.13 (s, 1H), 13.38 (s, 1H); LC-MS: 449.1 (MH+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08101608B2
Quelldatensatzuspto-grants-2012_01
ORD IDord-50bffd2ee01841a18210610b8347474a
Quellennotizuspto-grants-2012_01