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887147-19-5

887147-19-5 Structure

887147-19-5 Structure
IdentificationBack 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 PropertiesBack 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
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H312-H332
[Precautionary statements ]

P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P330-P363-P501
[HS Code ]

2933998090
Spectrum DetailBack Directory
[Spectrum Detail]

4,6-dichloro-1-Methyl-1H-iMidazo[4,5-c]pyridine(887147-19-5)1HNMR
Hazard InformationBack Directory
[Synthesis]

1H-Imidazo[4,5-c]pyridin-7-amine,4,6-dichloro-1-methyl-(9CI)

805316-72-7

4,6-dichloro-1-Methyl-1H-iMidazo[4,5-c]pyridine

887147-19-5

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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