反应 #1616608
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openreactiondata ↗doi:10.6084/m9.figshare.5104873.v1; patent:US08962627B2
反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: N-(4-Fluoro-phenyl)-2-{4-hydroxyimino-2-pyrrolo[1,2-c]pyrimidin-3-yl-4H-chromen-6-yloxy}-acetamide was prepared in 41% overall yield using the method described in example 147, starting from 6-hydroxy-2-pyrrolo[1,2-c]pyrimidin-3-yl-chromen-4-one O-tert-butyl-oxime (example 81A) and 2-Bromo-N-(4-fluoro-phenyl)-acetamide (Bioorg. Med. Chem. 11 (2003) 2769-2782). overall yield
来源 ID: ord-60a21aedb9b94bce8eb3cbf75cdd4581