Sodium Azide → 4'-[5-(azidomethyl)-1,3,4-oxadiazol-2-yl]-N-cyclopropyl-5-fluoro-6-methyl-1,1'-biphenyl-3-carboxamide
反応式
[N-:1]=[N+:2]=[N-:3].[Na+].Cl[CH2:6][C:7]1[O:11][C:10]([C:12]2[CH:17]=[CH:16][C:15]([C:18]3[C:23]([CH3:24])=[C:22]([F:25])[CH:21]=[C:20]([C:26]([NH:28][CH:29]4[CH2:31][CH2:30]4)=[O:27])[CH:19]=3)=[CH:14][CH:13]=2)=[N:9][N:8]=1>O.CN(C=O)C.C(O)C>[N:1]([CH2:6][C:7]1[O:11][C:10]([C:12]2[CH:17]=[CH:16][C:15]([C:18]3[C:23]([CH3:24])=[C:22]([F:25])[CH:21]=[C:20]([C:26]([NH:28][CH:29]4[CH2:30][CH2:31]4)=[O:27])[CH:19]=3)=[CH:14][CH:13]=2)=[N:9][N:8]=1)=[N+:2]=[N-:3]参加物
6
反応物 2
生成物 1
試薬・触媒・溶媒 3
反応条件
- 温度
- 90 °C
実験手順
A solution of sodium azide (40 mg) in water (3.5 ml) was added to (4′-[5-(chloromethyl)-1,3,4-oxadiazol-2-yl]-N-cyclopropyl-5-fluoro-6-methyl-1,1′-biphenyl-3-carboxamide (Intermediate 34) (200 mg) in DMF (1.5 ml) and ethanol (7 ml) and the reaction mixture stirred for 5 hours at 90° C. The reaction was concentrated under vacuum and the residue partitioned between water (15 ml) and chloroform (15 ml) and the aqueous extracted with chloroform (2×15 ml). The combined organic extracts were dried (magnesium sulphate), and the solvent evaporated under vacuum to give 4′-[5-(azidomethyl)-1,3,4-oxadiazol-2-yl]-N-cyclopropyl-5-fluoro-6-methyl-1,1′-biphenyl-3-carboxamide.
後処理
- concentrationThe reaction was concentrated under vacuum
- customthe residue partitioned between water (15 ml) and chloroform (15 ml)
- extractionthe aqueous extracted with chloroform (2×15 ml)
- dry with materialThe combined organic extracts were dried (magnesium sulphate)
- customthe solvent evaporated under vacuum
出典と根拠
- ORDレコード
- ord-5342d0f3f4284b378fcff678151285a4
- 出典データセット
- uspto-grants-2008_09
- 特許番号
- US07425555B2
反応ノート
読み込み中…