Potassium Carbonate → (2R,5R)-5-(6-bromo-3-fluoro-pyridin-2-yl)-2,5-dimethyl-2-trifluoromethyl-5,6-dihydro-2H-[1,4]oxazin-3-ylamine
反応式
[Br:1][C:2]1[N:7]=[C:6]([C@:8]([NH:20]S(C2C=CC([N+]([O-])=O)=CC=2)(=O)=O)([CH3:19])[CH2:9][O:10][C@@:11]([C:17]#[N:18])([CH3:16])[C:12]([F:15])([F:14])[F:13])[C:5]([F:33])=[CH:4][CH:3]=1.C(N[C@H](C(O)=O)CS)(=O)C.C([O-])([O-])=O.[K+].[K+]>C(O)C>[Br:1][C:2]1[N:7]=[C:6]([C@:8]2([CH3:19])[CH2:9][O:10][C@@:11]([CH3:16])([C:12]([F:15])([F:14])[F:13])[C:17]([NH2:18])=[N:20]2)[C:5]([F:33])=[CH:4][CH:3]=1参加物
5
反応物 3
生成物 1
試薬・触媒・溶媒 1
反応条件
- 温度
- 80 °C
実験手順
A solution of N—[(R)-1-(6-bromo-3-fluoro-pyridin-2-yl)-2-((R)-1-cyano-2,2,2-trifluoro-1-methyl-ethoxy)-1-methyl-ethyl]-4-nitro-benzenesulfonamide (9.18 g, 16.53 mmol) and N-acetylcysteine (5.40 g, 33.10 mmol) in 92 ml ethanol was evacuated and flushed with nitrogen. K2CO3 (4.57 g, 33.1 mmol) was added and the mixture was stirred at 80° C. for 3 days. The reaction mixture was concentrated in vacuo to about ¼ of the original volume and partitioned between water and TBME. The organic layer was washed with 10% aq. K2CO3 solution, dried over Na2SO4, filtered and evaporated to give a yellow oil. Column chromatography on silica (hexanes/14-50% (EtOAc:MeOH 95:5)) gave 4.55 g of the title compound as an off-white solid.
後処理
- customflushed with nitrogen
- concentrationThe reaction mixture was concentrated in vacuo to about ¼ of the original volume
- custompartitioned between water and TBME
- washThe organic layer was washed with 10% aq. K2CO3 solution
- dry with materialdried over Na2SO4
- filtrationfiltered
- customevaporated
- customto give a yellow oil
出典と根拠
- ORDレコード
- ord-0e92ddde7ef343bd843aebd06a507ee5
- 出典データセット
- uspto-grants-2014_01
- 特許番号
- US08637508B2
反応ノート
読み込み中…