ChemicalBook--->CAS DataBase List--->1161847-36-4

1161847-36-4

1161847-36-4 Structure

1161847-36-4 Structure
IdentificationBack Directory
[Name]

6-Chloro-imidazo[1,2-b]pyridazin-8-ylamine
[CAS]

1161847-36-4
[Synonyms]

6-Chloroimidazo[1,2-b]pyridazin-8-amine
8-Amino-6-chloroimidazo[1,2-b]pyridazine
6-Chloro-imidazo[1,2-b]pyridazin-8-ylamine
Imidazo[1,2-b]pyridazin-8-amine, 6-chloro-
[Molecular Formula]

C6H5ClN4
[MDL Number]

MFCD21336327
[MOL File]

1161847-36-4.mol
[Molecular Weight]

168.58
Chemical PropertiesBack Directory
[density ]

1.71±0.1 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
[pka]

4.89±0.30(Predicted)
Spectrum DetailBack Directory
[Spectrum Detail]

6-Chloro-imidazo[1,2-b]pyridazin-8-ylamine(1161847-36-4)1HNMR
Hazard InformationBack Directory
[Synthesis]

Tert-butyl N-(6-chloroimidazo[1,2-b]pyridazin-8-yl)carbamate

1161847-35-3

6-Chloro-imidazo[1,2-b]pyridazin-8-ylamine

1161847-36-4

Tert-butyl (6-chloroimidazo[1,2-b]pyridazin-8-yl)carbamate (1.59 g, 5.91 mmol) was used as a raw material and dissolved in a mixture of 30 mL of dichloromethane and 15 mL of trifluoroacetic acid. After the reaction was completed, the solution was concentrated to a yellow oil. Subsequently, 50 mL of saturated aqueous sodium bicarbonate solution was slowly added for treatment. Undissolved solids were separated by filtration through a Brinell funnel and rinsed with plenty of water. Finally, drying by vacuum aspiration gave 1.10 g (102% crude yield) of 6-chloroimidazo[1,2-b]pyridazin-8-amine as a yellow solid, which can be used without further purification.

[References]

[1] Patent: WO2009/77334, 2009, A1. Location in patent: Page/Page column 85
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