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ChemicalBook CAS DataBase List Pemigatinib
1513857-77-6

Pemigatinib synthesis

6synthesis methods
Removal of the acetaldehyde protecting group in compound 284 under acidic conditions afforded aldehyde 285. Reductive amination of aldehyde 285 with aniline 286 gave benzylamine 287. Benzylamine 287 reacted with isocyanate 288 to form the desired urea 289. In the presence of a strong base, LHMDS (lithium dimethylsilane), compound 289 underwent intramolecular cyclization to displace the adjacent chlorine atom to yield azatricyclic compound 290. Conventional hydrolysis to remove the benzenesulfonyl group completed the construction of pemitinib, affording the final product in good yield.
Pemigatinib synthesis
958230-19-8 Synthesis
4-CHLORO-1H-PYRROLO[2,3-B]PYRIDINE-5-CARBALDEHYDE

958230-19-8
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Pemigatinib

1513857-77-6
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915403-16-6 Synthesis
4-(ethylamino)-1H-Pyrrolo[2,3-b]pyridine-5-carboxaldehyde

915403-16-6
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Pemigatinib

1513857-77-6
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