반응 #60693

ord-2b638aacce8e4dc78b66860ae6fd61a2

반응 조건

상세 조건
See reaction.notes.procedure_details.

실험 절차

Using deprotection method B, but without addition of anisole, 4-{2-[(3-chloro-1H-indole-6-carbonyl)amino]-2-(4-pyridinyl)ethoxymethyl}piperidine-1-carboxylic acid tert-butyl ester (83 mg, 0.16 mmol) afforded 67 mg (100%) of the title compound as a crude residue, which was used without further purification.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07427632B2uspto-grants-2008_09