Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1417069Generated: November 4, 2026

p-Anisoyl chloride → Pyridine, 4-[2-(4-methoxyphenyl)-1-methyl-4-phenyl-1H-imidazol-5-yl]-

https://huagongshe.com/reaction/1417069

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Anisoyl chlorideHCID 7477—
ReactantTriethylamineHCID 8471—
ReactantN-Methylpyridine-4-methylamineHCID 81436—
Reactant4-Methoxy-N-methyl-N-(4-picolyl)benzamideHCID 15407880—
SolventDichloromethaneHCID 6344—
ProductPyridine, 4-[2-(4-methoxyphenyl)-1-methyl-4-phenyl-1H-imidazol-5-yl]-HCID 1026889021%

Reaction Steps

4-Methoxy-N-methyl-N-(4-picolyl)benzamide--To a solution of N-methyl-N-(4-picolyl)amine (0.40 g, 3.3 mmol) and triethylamine (1.5 mL, 10.8 mmol) in CH2Cl2 (15 mL) was added 4-methoxybenzoyl chloride (1.2 g, 7.3 mmol). The resulting mixture was stirred at rt for 15 min, and then partitioned between 2.5N NaOH and Et2O. The organic extract was washed with saturated aqueous NaCl and dried (MgSO4). The solvent was removed in vacito, and the residue was purified by flash chromatography, eluting with a solvent gradient of 2-4% MeOH/CHCl3. The material that was isolated was triturated with Et2O to provide the title compound as a light yellow solid (0.18 g, 21%): 1H NMR (CDCl3): d 8.60 (d, 2H); 7.43 (brd, 2H); 7.20 (br s, 2H); 6.90 (br d, 2H); 4.66 (br s, 2H); 3.80 (s, 3H); 3.00 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05916891
Source datasetuspto-grants-1999_06
ORD IDord-a1fed4315f93413787ef309f007ac1ce
Source noteuspto-grants-1999_06