5-[(4-methylphenyl)sulfonyl]-5H-Pyrrolo[2,3-b]pyrazin-2-amine

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5-[(4-methylphenyl)sulfonyl]-5H-Pyrrolo[2,3-b]pyrazin-2-amine Basic information
Product Name:5-[(4-methylphenyl)sulfonyl]-5H-Pyrrolo[2,3-b]pyrazin-2-amine
Synonyms:2-Amino-5-tosyl-5H-pyrrolo[2,3-b]pyrazine;5-[(4-methylphenyl)sulfonyl]-5H-Pyrrolo[2,3-b]pyrazin-2-amine;5H-Pyrrolo[2,3-b]pyrazin-2-amine, 5-[(4-methylphenyl)sulfonyl]-;5-tosyl-5H-pyrrolo[2,3-b]pyrazin-2-amin;Upadacitinib Intermediate3;Upadacitinib Impurity 17;Upatinib impurity 46;Upadacitinib Impurity 46
CAS:1201187-46-3
MF:C13H12N4O2S
MW:288.33
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Mol File:1201187-46-3.mol
5-[(4-methylphenyl)sulfonyl]-5H-Pyrrolo[2,3-b]pyrazin-2-amine Structure
5-[(4-methylphenyl)sulfonyl]-5H-Pyrrolo[2,3-b]pyrazin-2-amine Chemical Properties
Boiling point 519.0±60.0 °C(Predicted)
density 1.49±0.1 g/cm3(Predicted)
storage temp. Store at Room Tem.
pka3.20±0.30(Predicted)
Safety Information
MSDS Information
5-[(4-methylphenyl)sulfonyl]-5H-Pyrrolo[2,3-b]pyrazin-2-amine Usage And Synthesis
Uses5-[(4-Methylphenyl)sulfonyl]-5H-Pyrrolo[2,3-b]pyrazin-2-amine functions as a reagent in the ligand-controlled and iridium-catalyzed preparation of imidazo[1,2-a]pyrrolo[2,3-e]pyrazines or β-keto amines via reaction of sulfoxonium ylides with 2-amino heterocycles.
5-[(4-methylphenyl)sulfonyl]-5H-Pyrrolo[2,3-b]pyrazin-2-amine Preparation Products And Raw materials
Preparation ProductsN-Tosyl-5-bromo-4,7-diazaindole
Tag:5-[(4-methylphenyl)sulfonyl]-5H-Pyrrolo[2,3-b]pyrazin-2-amine(1201187-46-3) Related Product Information
(3R,4S)-1-((Benzyloxy)carbonyl)-4-ethylpyrrolidine-3-carboxylic acid ABT-494 ENANTIOMER (3R,4S)-3-(2-Bromoacetyl)-4-ethyl-1-pyrrolidinecarboxylic acid phenylmethyl ester (3R,4S)-1-[(benzyloxy)carbonyl]-4-ethylpyrrolidine-3-carboxylic acid tert-butyl 5-tosyl-5H-pyrrolo[2,3-b]pyrazin-2-ylcarbamate N-Tosyl-5-bromo-4,7-diazaindole