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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1514902Generated: October 30, 2026

2-Aminoquinoline → HCID 66965562, compound

https://huagongshe.com/reaction/1514902

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminoquinolineHCID 11379—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 86651262HCID 86651262—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66965562HCID 66965562—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a stirred suspension of 2-(2-chloro-6-trifluoromethylphenyl)-3H-benzoimidazole-5-carbonyl chloride (394 mg, 1.0 mmol) and quinolin-2-ylamine (144 mg, 1.0 mmol) in THF (6 mL) was added DIPEA (0.53 ml, 3.0 mmol). The solution was heated at 60° C. for 2 days and the reaction was quenched with water and 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 (1:4) as eluent to give 2-(2-chloro-6-trifluoromethylphenyl)-3H-benzoimidazole-5-carboxylic acid quinolin-2-ylamide as a white solid. 1H NMR (Methanol-d4, 400 MHz): δ 8.45 (d, 1H), 8.37 (d, 1H), 8.08 (d, 1H), 7.94 (m, 4H), 7.83 (m, 1H), 7.74 (m, 1H), 7.54 (m, 1H). MS (m/z) 467.1 (M+1); Retention time: 1.45 min (Method 10).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08222248B2
Source datasetuspto-grants-2012_07
ORD IDord-5d9b9cb3ae814e679b8eef17cab67ae7
Source noteuspto-grants-2012_07