反応式
[Cl:1][C:2]1[CH:9]=[C:8](F)[CH:7]=[CH:6][C:3]=1[C:4]#[N:5].Cl.[CH2:12]([O:16][C:17](=[O:21])[CH:18]([CH3:20])[NH2:19])[CH:13]([CH3:15])[CH3:14]>>[CH2:12]([O:16][C:17](=[O:21])[C@H:18]([CH3:20])[NH:19][C:8]1[CH:7]=[CH:6][C:3]([C:4]#[N:5])=[C:2]([Cl:1])[CH:9]=1)[CH:13]([CH3:15])[CH3:14]参加物
3
実験手順
Following General Procedure AP above and using 2-chloro-4-fluorobenzonitrile (Aldrich) and D,L-alanine iso-butyl ester hydrochloride (from Example AA above), the title compound was prepared. The product was recovered by column chromatography on silica gel using 1:5 EtOAc/hexanes as the eluant.
後処理
- customThe product was recovered by column chromatography on silica gel using 1:5 EtOAc/hexanes as the eluant
出典と根拠
- ORDレコード
- ord-b417a860cdef47898322d20ece20b974
- 出典データセット
- uspto-grants-2008_06
- 特許番号
- US07390801B2
関連ノート
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