After forming the pyrrolo[2,3-d]pyrimidine ring, introduce the amino group at the 2-position and the keto group at the 4-position. This can be achieved through various synthetic methods, including reductive amination and oxidation reactions.
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2-[4-({[2-(2,2-dimethyl-propionylamino)-6-methyl-4-oxo-4,7-dihydro-3H-pyrrolo[2,3-d]pyrimidin-5-ylmethyl]-amino}-methyl)-benzoylamino]-pentanedioic acid
