反応式
[CH3:1][O:2][C:3](=[O:15])[C:4]1[CH:9]=[C:8]([C:10]([F:13])([F:12])[F:11])[CH:7]=[C:6]([SH:14])[CH:5]=1.C(N(CC)C(C)C)(C)C.Br[CH2:26][CH2:27][CH2:28][C:29]([O:31][C:32]([CH3:35])([CH3:34])[CH3:33])=[O:30].C(OCC)(=O)C>C(#N)C>[CH3:1][O:2][C:3](=[O:15])[C:4]1[CH:9]=[C:8]([C:10]([F:12])([F:13])[F:11])[CH:7]=[C:6]([S:14][CH2:26][CH2:27][CH2:28][C:29]([O:31][C:32]([CH3:35])([CH3:34])[CH3:33])=[O:30])[CH:5]=1参加物
反応物 4
生成物 1
試薬・触媒・溶媒 1
実験手順
To a solution of 3-mercapto-5-trifluoromethyl-benzoic acid methyl ester (990 mg, 4.19 mmol) in acetonitrile (25 mL) were added N,N-diisopropylethylamine (1.08 g, 1.46 mL, 8.38 mmol) and tert-butyl 4-bromobutanoate (935 mg, 4.19 mmol, CAS RN 110611-91-1). The clear yellow solution was stirred at room temperature for 2.5 hours and then poured on water and ethyl acetate and the layers were separated. The aqueous layer was extracted twice with ethyl acetate. The organic layers were washed with brine, dried over magnesium sulfate, filtered, treated with silica gel and evaporated. The compound was purified by silica gel chromatography on a 50 g column using a MPLC system (CombiFlash Companion, Isco Inc.) eluting with a gradient of n-heptane:ethyl acetate (100:0 to 70:30). Light yellow liquid (1.27 g, 80%). MS (ESI+): m/z=379 ([M+]).
後処理
- customthe layers were separated
- extractionThe aqueous layer was extracted twice with ethyl acetate
- washThe organic layers were washed with brine
- dry with materialdried over magnesium sulfate
- filtrationfiltered
- additiontreated with silica gel
- customevaporated
- customThe compound was purified by silica gel chromatography on a 50 g column
- washeluting with a gradient of n-heptane:ethyl acetate (100:0 to 70:30)
出典と根拠
- ORDレコード
- ord-448051f2358b4aeab4e59db3d63c93fb
- 出典データセット
- uspto-grants-2014_06
- 特許番号
- US08748434B2
関連ノート
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