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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;5-Tosyl-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;Upadacitinib Impurity 46 | CAS: | 1201187-46-3 | MF: | C13H12N4O2S | MW: | 288.33 | EINECS: | | Product Categories: | | Mol File: | 1201187-46-3.mol | |
| 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) | pka | 3.20±0.30(Predicted) |
| 5-[(4-methylphenyl)sulfonyl]-5H-Pyrrolo[2,3-b]pyrazin-2-amine Usage And Synthesis |
Uses | 5-[(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 |
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