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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,4,6-Trichlorobenzaldehyde | HCID 5314457 | — |
| Reactant | 3,4-diamino-N-quinolin-2-yl-benzamide | HCID 66965740 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 2-(2,4,6-Trichlorophenyl)-3H-benzoimidazole-5-carboxylic acid quinolin-2-ylamide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08222248B2 |
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| Source dataset | uspto-grants-2012_07 |
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| ORD ID | ord-de7ae132a5df4fdba741aa9bfbf1517a |
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| Source note | uspto-grants-2012_07 |
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