Hydrochloric Acid → (4-Ethyl-2-methyl-1,3-thiazol-5-yl)methanol
反応式
[CH2:1]([C:3]1[N:4]=[C:5]([CH3:11])[S:6][C:7]=1[C:8](O)=[O:9])[CH3:2].Cl>C1COCC1>[CH2:1]([C:3]1[N:4]=[C:5]([CH3:11])[S:6][C:7]=1[CH2:8][OH:9])[CH3:2]参加物
4
実験手順
To a borane tetrahydrofuran complex solution (1.2 M in THF, 5 mL) was added 4-ethyl-2-methylthiazole-5-carboxylic acid (400 mg) at 0° C. The mixture was stirred at 0° C. to room temperature under argon atmosphere overnight. To the mixture was added 1N HCl at room temperature, and the mixture was extracted with EtOAc. The organic layer was separated, washed successively with brine and water, dried over Na2SO4 and concentrated in vacuo. The residue was purified by silica gel column chromatography (EtOAc/hexane) to give the title compound (125 mg).
後処理
- extractionthe mixture was extracted with EtOAc
- customThe organic layer was separated
- washwashed successively with brine and water
- dry with materialdried over Na2SO4
- concentrationconcentrated in vacuo
- customThe residue was purified by silica gel column chromatography (EtOAc/hexane)
出典と根拠
- ORDレコード
- ord-0c58eb5110d94b3c996c563aa287aedd
- 出典データセット
- uspto-grants-2016_01
- 特許番号
- US09238639B2
反応ノート
読み込み中…