반응 #2452614

ord-10c3c653341744c19f6d833dfe34686b

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타Purification by preparative TLC

실험 절차

The title compound was synthesized by the hydrogen chloride mediated deprotection of N-benzyl-N-(2-((tert-butyldimethylsilyl)oxy)ethyl)-3-(4-phenyl-1H-pyrazol-5-yl)-1H-pyrrolo[2,3-b]pyridin-6-amine as described in Step 2 of Example 5. Purification by preparative TLC then preparative HPLC, followed by salt formation with 2N HCl/MeOH and final isolation by lyophilization from water afforded 2-{benzyl-[3-(4-phenyl-2H-pyrazol-3-yl)-1H-pyrrolo[2,3-b]pyridin-6-yl]-amino}ethanol dihydrochloride in 10% overall yield as a yellow solid.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08697697B2uspto-grants-2014_04