반응 #2513861

ord-0a34dc2f0ebb49d4a00f45805b3b19e0

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    여과The reaction was worked up by filtration through a syringe
  2. 2
    여과filter
  3. 3
    농축concentrated
  4. 4
    기타the crude product was purified by preparative HPLC
  5. 5
    기타This resulted in the product with the molecular weight of 471.6 (C29H33N3O3)

실험 절차

5-Bromofuran-2-carboxylic acid [4-(3-dimethylaminopyrrolid in-1-yl)phenyl]amide (75 mg) was dissolved together with 1-butoxy-4-ethynylbenzene (35 mg) in N,N-dimethylformamide (1 ml) and, under argon, added dropwise to a suspension of Pd(tBu3P)2Cl2 (4 mg), copper (I) iodide (75 mg) and N,N-diisopropylamine (20 mg) in anhydrous tetrahydrofuran (3 ml). The mixture was stirred at room temperature for 8 hours. The reaction was worked up by filtration through a syringe filter and concentrated, and the crude product was purified by preparative HPLC. This resulted in the product with the molecular weight of 471.6 (C29H33N3O3); MS (ESI): 472 (M+H+) as hydrotrifluoroacetate.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07968550B2uspto-grants-2011_06