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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 422014Generated: October 25, 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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrrole-2-carboxaldehydeHCID 13854—
Reactant2-oxo-2,3-dihydro-1H-indole-6-carboxylic acid (3-benzoylamino-phenyl)-amideHCID 66675495—
CatalystPiperidineHCID 8082—
SolventEthanolHCID 702—
Product2-Oxo-3-(1h-pyrrol-2-ylmethylene)-2,3-dihydro-1h-indole-6-carboxylic acid (3-benzoylamino-phenyl)-amideHCID 66674790—

Reaction Steps

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+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101608B2
Source datasetuspto-grants-2012_01
ORD IDord-50bffd2ee01841a18210610b8347474a
Source noteuspto-grants-2012_01