反应详情

The title compound was prepared according to the method described for Example 1 using (2-Amino-7-tert-butyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl)-(5-amino-pyridin-3-yl)-methanone (see Preparation 65) and (4-cyclopropyl-pyrazol-1-yl)-acetic acid to afford the title compound as a pale yellow solid in 16% yield, 12 mg. LCMS (System 10): Rt=2.80 min; m/z 459 [M+H]+.

1. customThe title compound was prepared