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

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6-Chloro-imidazo[1,2-b]pyridazin-8-ylamine Basic information
Product Name:6-Chloro-imidazo[1,2-b]pyridazin-8-ylamine
Synonyms:6-Chloro-imidazo[1,2-b]pyridazin-8-ylamine;6-Chloroimidazo[1,2-b]pyridazin-8-amine;Imidazo[1,2-b]pyridazin-8-amine, 6-chloro-;8-Amino-6-chloroimidazo[1,2-b]pyridazine
CAS:1161847-36-4
MF:C6H5ClN4
MW:168.58
EINECS:
Product Categories:
Mol File:1161847-36-4.mol
6-Chloro-imidazo[1,2-b]pyridazin-8-ylamine Structure
6-Chloro-imidazo[1,2-b]pyridazin-8-ylamine Chemical Properties
density 1.71±0.1 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
pka4.89±0.30(Predicted)
Safety Information
MSDS Information
6-Chloro-imidazo[1,2-b]pyridazin-8-ylamine Usage And Synthesis
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
6-Chloro-imidazo[1,2-b]pyridazin-8-ylamine Preparation Products And Raw materials
Raw materialsTert-butyl N-(6-chloroimidazo[1,2-b]pyridazin-8-yl)carbamate-->Sodium bicarbonate-->Dichloromethane-->Water-->Trifluoroacetic acid
Tag:6-Chloro-imidazo[1,2-b]pyridazin-8-ylamine(1161847-36-4) Related Product Information
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