반응 #715640

ord-b759d7987dc54f96a90fef3b7ee8e42f

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타the product was purified by preparative HPLC-MS (Waters XBridge C18
  2. 2
    세척eluting with a gradient of MeCN/H2O containing 0.15% NH4OH)

실험 절차

To a suspension of 6-benzyl-1,7-dimethyl-6H-pyrrolo[2,3-e][1,2,4]triazolo[4,3-a]pyridin-4-amine (32.0 mg, 0.110 mmol, from Step 3) in tetrahydrofuran (1 mL) was added acetyl chloride (15.1 μL, 0.213 mmol, Aldrich) and N,N-diisopropylethylamine (76 μL, 0.44 mmol). After 3.5 hours, the product was purified by preparative HPLC-MS (Waters XBridge C18, eluting with a gradient of MeCN/H2O containing 0.15% NH4OH). Yield: (19 mg, 52%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US09309246B2uspto-grants-2016_04