反応 #40628

ord-23ec465f1d48481894c1f7294e49f135

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    濃縮the solution was concentrated
  2. 2
    workup.DISSOLUTIONthe crude residue was redissolved in dichloromethane (10 mL)
  3. 3
    workup.WAITAfter 15 h
  4. 4
    その他the reaction mixture was partitioned between water and dichloromethane
  5. 5
    その他the organic layer was separated
  6. 6
    乾燥dried (MgSO4)
  7. 7
    濃縮concentrated

実験手順

Bromine (0.15 g, 0.94 mmol) was added to a solution of 8-cyclohexyl-2-methylsulfanyl-5-oxo-5,6,7,8-tetrahydro-pyrido[2,3-d]pyrimidine-6-carboxylic acid ethyl ester (0.28 g, 0.79 mmol) in dichloromethane (10 mL). After 5 min, the solution was concentrated and the crude residue was redissolved in dichloromethane (10 mL) and diisopropylethylamine (0.42 mL, 2.4 mmol) was added. After 15 h, the reaction mixture was partitioned between water and dichloromethane, the organic layer was separated, dried (MgSO4) and concentrated to provide 0.28 g (87%) of the title compound. Mass Spectrum (LCMS, ESI pos.) Calcd. For C17H21N3O3S: 347.13. found: (M+H) 348.3.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07728003B2uspto-grants-2010_06