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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1514915Generated: October 25, 2026

2,4,6-Trichlorobenzaldehyde → 2-(2,4,6-Trichlorophenyl)-3H-benzoimidazole-5-carboxylic acid quinolin-2-ylamide

https://huagongshe.com/reaction/1514915

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4,6-TrichlorobenzaldehydeHCID 5314457—
Reactant3,4-diamino-N-quinolin-2-yl-benzamideHCID 66965740—
SolventDimethyl SulfoxideHCID 679—
Product2-(2,4,6-Trichlorophenyl)-3H-benzoimidazole-5-carboxylic acid quinolin-2-ylamideHCID 66965619—

Reaction Steps

To a stirred solution of 2,4,6-trichlorobenzaldehyde (150 mg, 0.72 mmol) and 3,4-diamino-N-quinolin-2-yl-benzamide (200 mg, 0.72 mmol) in DMSO (10 mL) was added FeCl3 (23 mg, 0.14 mmol). The solution was stirred at ambient temperature for 2 days. The reaction was quenched with water and the aqueous layer was extracted with EtOAc. The organic layer was washed with water, brine, dried with MgSO4, and filtered. The solvent was removed under reduced pressure and the residue was purified by flash chromatography using heptane/EtOAc (1/3) as eluent to give the title compound as a white solid. 1H NMR (Methanol-d4, 400 MHz): δ 8.45 (m, 3H), 8.08 (d, 1H), 7.93 (m, 2H), 7.85 (s, 1H), 7.76 (s, 2H), 7.75 (m, 1H), 7.55 (m, 1H). MS (m/z) 467.0 (M+1); Retention time: 1.48 min (Method 10).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08222248B2
Source datasetuspto-grants-2012_07
ORD IDord-de7ae132a5df4fdba741aa9bfbf1517a
Source noteuspto-grants-2012_07