Lithium Hydroxide → HCID 57457166、化合物
反応式
[CH3:1][O:2][C:3]1[C:19]([C:20]([F:23])([F:22])[F:21])=[CH:18][C:6]2[N:7]([CH2:12][C:13]([O:15]CC)=[O:14])[C:8](=[O:11])[CH2:9][O:10][C:5]=2[CH:4]=1.[Li+].[OH-].CC#N.O.FC(F)(F)C(O)=O>O1CCCC1.O>[CH3:1][O:2][C:3]1[C:19]([C:20]([F:23])([F:21])[F:22])=[CH:18][C:6]2[N:7]([CH2:12][C:13]([OH:15])=[O:14])[C:8](=[O:11])[CH2:9][O:10][C:5]=2[CH:4]=1参加物
実験手順
Ethyl [7-(methyloxy)-3-oxo-6-(trifluoromethyl)-2,3-dihydro-4H-1,4-benzoxazin-4-yl]acetate (0.36 g, 1.1 mmol) was dissolved in 4 mL of tetrahydrofuran and treated with a solution of LiOH (0.028 g, 1.2 mmol) dissolved in 0.5 mL of water. The reaction was stirred vigorously at room temperature for 18 hours before it was determined to be complete by LCMS (two Aquasil C18, 20×1 mm columns were run in sequence, 4 minutes at 0.1 mL/min, 1-99% CH3CN/H2O with 0.018% trifluoroacetic acid, ES) Rt=1.62 min and m/e 306 [M+1]+. The solvent was removed by rotary evaporation and the residue was then dissolved in 50 mL of ethyl acetate. The organic layer was washed with a 10% hydrochloric acid solution (3×10 mL) and the organic phase was then dried over Na2SO4, filtered and concentrated to give [7-(methyloxy)-3-oxo-6-(trifluoromethyl)-2,3-dihydro-4H-1,4-benzoxazin-4-yl]acetic acid (0.31 g, 1.0 mmol, 91%) as an off-white amorphous solid. MS (ES) m/e 306 [M+H]+.
後処理
- customThe solvent was removed by rotary evaporation
- dissolutionthe residue was then dissolved in 50 mL of ethyl acetate
- washThe organic layer was washed with a 10% hydrochloric acid solution (3×10 mL)
- dry with materialthe organic phase was then dried over Na2SO4
- filtrationfiltered
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-132353bbd3054583aab3e56df6c1443a
- 出典データセット
- uspto-grants-2008_10
- 特許番号
- US07432258B2
反応ノート
読み込み中…