反応 #636795

ord-3c1531d13a934f11a07d83700f94f577

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-cyclopentyloxy-phenylsulfanyl)-2-methyl-phenoxy]-acetic acid ethyl ester (300 mg; 0.63 mmol), phenylacetylen (191.7 mg; 1.88 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: 200 mg (64%). HPLC-MS: m/z: 500.8 (M)+; Rt: 3.30 min.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07943669B2uspto-grants-2011_05