| Identification | Back Directory | [Name]
4,6-dichloro-1-Methyl-1H-iMidazo[4,5-c]pyridine | [CAS]
887147-19-5 | [Synonyms]
4,6-dichloro-1-Methyl-1H-iMidazo[4,5-c]pyridine 1H-Imidazo[4,5-c]pyridine, 4,6-dichloro-1-methyl- | [Molecular Formula]
C7H5Cl2N3 | [MDL Number]
MFCD21603853 | [MOL File]
887147-19-5.mol | [Molecular Weight]
202.04 |
| Chemical Properties | Back Directory | [Boiling point ]
367.5±52.0 °C(Predicted) | [density ]
1.60±0.1 g/cm3(Predicted) | [storage temp. ]
Inert atmosphere,2-8°C | [pka]
1.86±0.30(Predicted) | [Appearance]
Yellow to brown Solid |
| Hazard Information | Back Directory | [Synthesis]
General procedure for the synthesis of 4,6-dichloro-1-methyl-1H-imidazo[4,5-c]pyridin-7-amine from 4,6-dichloro-1-methyl-1H-imidazo[4,5-c]pyridine: a solution of sodium nitrite (5.28 g, 76.5 mmol) in water (17 mL) was added dropwise over 5 min to a stirred 4,6-dichloro-1-methyl-1H-imidazo and [4,5-c]pyridin-7-amine (11.3 g, 52 mmol) solution of hypophosphorous acid (50 wt.% aqueous solution, 150 mL), keeping the reaction temperature between 0°C and 50°C. The reaction mixture was gradually warmed to room temperature and stirring was continued for 40 minutes. Subsequently, the mixture was cooled in an ice bath to between 0 °C and 50 °C, and the pH was adjusted to >10 by addition of aqueous sodium hydroxide (55 g dissolved in 100 mL of water). the resulting suspension was filtered, and the filter cake was washed with water and dried by suction to afford the product 4,6-dichloro-1-methyl-1H-imidazo[4,5-c]pyridine (9.9 g, 97% yield), which was analyzed for purity by high performance liquid chromatography ( HPLC) analyzing the purity was 99%, retention time was 0.92 min, and the molecular ion peak (M+H)+ detected by LC/MS was 202.06 (204.04,206.02). | [References]
[1] Bioorganic and Medicinal Chemistry Letters, 2009, vol. 19, # 10, p. 2646 - 2649 [2] Patent: WO2006/122137, 2006, A1. Location in patent: Page/Page column 71 [3] Patent: WO2006/53166, 2006, A1. Location in patent: Page/Page column 57 |
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