反応 #1600364

ord-f5797325db4f46d49183a6d239a06d91

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他The crude product was purified by preparative HPLC (method B)

実験手順

The title product was prepared from [4-(3-Bromo-5-isobutoxy-benzylsulfanyl)-2-methyl-phenoxy]-acetic acid ethyl ester (300 mg; 0.64 mmol) and phenylacetylene (262 mg; 2.6 mmol) applying the procedure described for {4-[3-[2-(4-Chloro-phenyl)-ethoxy]-5-(4-hydroxymethyl-phenylethynyl)-phenylsulfanyl]-2-methyl-phenoxy}-acetic acid ethyl ester. The crude product was purified by preparative HPLC (method B). Yield: 130 mg (45%). HPLC-MS: m/z: 489.1 (M+H)+; Rt: 3.01 min

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08217086B2uspto-grants-2012_07