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5-BROMO-1H-PYRAZOLO[3,4-B]PYRIDIN-3-YLAMINE

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Products Intro: Product Name:5-BROMO-1H-PYRAZOLO[3,4-B]PYRIDIN-3-YLAMINE
CAS:405224-24-0
Purity:95%-98% Package:1KG;5USD
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Products Intro: Product Name:5-Bromo-1H-pyrazolo[3,4-b]pyridin-3-amine
CAS:405224-24-0
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-07342
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CAS:405224-24-0
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Products Intro: Product Name:5-bromo-1H-pyrazolo[3,4-b]pyridin-3-amine
CAS:405224-24-0
Purity:0.97 Package:1KG;25KG
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Products Intro: Product Name:5-Bromo-1H-pyrazolo[3,4-b]pyridin-3-amine
CAS:405224-24-0
Purity:98% Package:5g,10g

5-BROMO-1H-PYRAZOLO[3,4-B]PYRIDIN-3-YLAMINE manufacturers

5-BROMO-1H-PYRAZOLO[3,4-B]PYRIDIN-3-YLAMINE Basic information
Uses
Product Name:5-BROMO-1H-PYRAZOLO[3,4-B]PYRIDIN-3-YLAMINE
Synonyms:5-BROMO-1H-PYRAZOLO[3,4-B]PYRIDIN-3-YLAMINE;3-Amino-5-bromo-1H-pyrazolo[3,4-B]pyridine;3-Amino-5-bromo-1H-pyrazo...;5-Bromo-1H-pyrazolo[3,4-b]pyridin-3-amine, 3-Amino-7-aza-5-bromo-1H-indazole;1H-Pyrazolo[3,4-b]pyridin-3-aMine,5-broMo-;5-Bromo-1H-pyrazole[3,4-b]pyridin-3-amine;5-bromo-1H-pyrazolo[3,4-b]pyridine-3-amine;5-Bromo-1H-pyrazolo[3,4-b]pyridin-ylamine
CAS:405224-24-0
MF:C6H5BrN4
MW:213.03
EINECS:
Product Categories:
Mol File:405224-24-0.mol
5-BROMO-1H-PYRAZOLO[3,4-B]PYRIDIN-3-YLAMINE Structure
5-BROMO-1H-PYRAZOLO[3,4-B]PYRIDIN-3-YLAMINE Chemical Properties
Boiling point 429.1±40.0 °C(Predicted)
density 1.994
storage temp. 2-8°C(protect from light)
pka9.55±0.40(Predicted)
form solid
AppearanceLight yellow to yellow Solid
InChIInChI=1S/C6H5BrN4/c7-3-1-4-5(8)10-11-6(4)9-2-3/h1-2H,(H3,8,9,10,11)
InChIKeySSNUTEUZXZIYTB-UHFFFAOYSA-N
SMILESC12NN=C(N)C1=CC(Br)=CN=2
Safety Information
Hazard Codes Xn
Risk Statements 22
HS Code 2933399990
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
MSDS Information
5-BROMO-1H-PYRAZOLO[3,4-B]PYRIDIN-3-YLAMINE Usage And Synthesis
Uses3-Amino-5-bromo-1H-pyrazolo[3,4-B]pyridine is an organic intermediate.
Synthesis
5-Bromo-2-chloro-3-cyanopyridine

405224-23-9

5-BROMO-1H-PYRAZOLO[3,4-B]PYRIDIN-3-YLAMINE

405224-24-0

General procedure for the synthesis of 3-amino-5-bromo-1H-pyrazolo[3,4-b]pyridine from 5-bromo-2-chloronicotinonitrile: Compound 3 (5-bromo-2-chloronicotinonitrile, 307 mg, 1.4 mmol) was dissolved in ethanol (10 mL) in a microwave reactor tube, followed by the addition of 5 equiv. of hydrazine hydrate (NH2NH2-H2O) to the solution. The reaction mixture was placed in a microwave reactor and radiated at 170 °C for 10 min. Upon completion of the reaction, the solvent was removed by rotary evaporator to afford the target product 3-amino-5-bromo-1H-pyrazolo[3,4-b]pyridine (4) in quantitative yield.

References[1] Patent: WO2007/59219, 2007, A1. Location in patent: Page/Page column 54-55
[2] Patent: WO2016/26549, 2016, A1. Location in patent: Page/Page column 43
[3] Bioorganic and Medicinal Chemistry Letters, 2013, vol. 23, # 20, p. 5578 - 5585
[4] Bioorganic and Medicinal Chemistry Letters, 2003, vol. 13, # 9, p. 1577 - 1580
[5] Patent: WO2013/42035, 2013, A1. Location in patent: Page/Page column 17
5-BROMO-1H-PYRAZOLO[3,4-B]PYRIDIN-3-YLAMINE Preparation Products And Raw materials
Raw materials5-Bromo-2-chloro-3-cyanopyridine-->5-Bromo-3-cyano-2-methoxypyridine-->Ethanol-->HYDRAZINE
Tag:5-BROMO-1H-PYRAZOLO[3,4-B]PYRIDIN-3-YLAMINE(405224-24-0) Related Product Information
3-Aminopyrazine-2-carboxylic acid 3-Nitro-1H-pyrazole Homopiperazine 1H-PYRAZOLO[3,4-B]PYRIDINE 5-BROMO-4,6-DIMETHYL-1H-PYRAZOLO[3,4-B]PYRIDIN-3-AMINE 5-BROMO-1H-PYRAZOLO[3,4-B]PYRIDIN-3-YLAMINE 5-BROMO-1H-PYRAZO[3,4-B]PYRIDINE

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