4-CHLORO-1-METHYL-1H-IMIDAZO[4,5-C]PYRIDINE
4-CHLORO-1-METHYL-1H-IMIDAZO[4,5-C]PYRIDINE Basic information
- Product Name:
- 4-CHLORO-1-METHYL-1H-IMIDAZO[4,5-C]PYRIDINE
- Synonyms:
-
- 4-CHLORO-1-METHYL-1H-IMIDAZO[4,5-C]PYRIDINE
- 4-Chloro-1-methyl-imidazo[4,5-c]pyridine
- 1H-Imidazo[4,5-c]pyridine, 4-chloro-1-methyl-
- CAS:
- 50432-68-3
- MF:
- C7H6ClN3
- MW:
- 167.6
- Product Categories:
-
- Heterocycle-Pyridine series
- Mol File:
- 50432-68-3.mol
4-CHLORO-1-METHYL-1H-IMIDAZO[4,5-C]PYRIDINE Chemical Properties
- Melting point:
- 168-170 °C(Solv: cyclohexane (110-82-7); ethyl acetate (141-78-6))
- Boiling point:
- 331.8±45.0 °C(Predicted)
- Density
- 1.43±0.1 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- pka
- 3.13±0.30(Predicted)
- Appearance
- Light brown to black Solid
4-CHLORO-1-METHYL-1H-IMIDAZO[4,5-C]PYRIDINE Usage And Synthesis
Synthesis
2770-01-6
74-88-4
50432-68-3
87034-78-4
NaH (78 mg, 1.95 mmol, 60% w/w oil solution) was slowly added to a solution of 4-chloro-3H-imidazo[4,5-c]pyridine (100 mg, 0.65 mmol) in DMF (3 mL) at 0 °C under nitrogen protection. The reaction mixture was stirred at 0 °C for 40 min. Subsequently, iodomethane (277 mg, 1.95 mmol) was added at the same temperature. The reaction mixture was warmed to room temperature and stirring was continued for 2 hours. Upon completion of the reaction, the reaction was quenched with saturated aqueous NH4Cl solution and extracted with ethyl acetate (20 mL x 3). The organic layers were combined, dried with anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was purified by preparative HPLC to afford 4-chloro-1-methyl-1H-imidazo[4,5-c]pyridine (58, 40.3 mg) and 4-chloro-3-methyl-3H-imidazo[4,5-c]pyridine (59, 41.0 mg), both yellow oils, respectively.LRMS (m/z): [M+H]+ calculated values 168.2, 170.2; measured values 168.0, 170.2.
References
[1] Patent: WO2016/101119, 2016, A1. Location in patent: Page/Page column 99; 100
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