Methanol → methyl (E)-2-(2-dimethylaminomethylidenaminothiazol-4-yl)-2-methoxyiminoacetate

HRID 1377951

反応式

HRID 1377951 の反応式
[Cl-].[CH3:2][N:3]([NH+]=CCl)[CH3:4].[NH2:8][C:9]1[S:10][CH:11]=[C:12](/[C:14](=[N:18]/[O:19][CH3:20])/C(O)=O)[N:13]=1.[CH3:21][OH:22].[C:23](=[O:26])([O-])O.[Na+].O1CCC[CH2:29]1>>[CH3:2][N:3]([CH:4]=[N:8][C:9]1[S:10][CH:11]=[C:12](/[C:14](=[N:18]/[O:19][CH3:20])/[C:21]([O:26][CH3:23])=[O:22])[N:13]=1)[CH3:29]

参加物

6

反応条件

温度
-3 °C

実験手順

Dimethylaminochloromethyleneammonium chloride (400 mg, 3.1 mmol) was dissolved in 10 ml of tetrahydrofuran, followed by cooling to -3° C. The solution was added with 300 mg (1.5 mmol) of (Z)-2-(2-aminothiazol-4-yl)-2-methoxyiminoacetic acid and the mixture so obtained was stirred for 40 minutes. After the resulting mixture was added with 10 ml of methanol and was then stirred for 10 minutes at room temperature, the mixture was poured into 50 ml of a saturated aqueous solution of sodium hydrogencarbonate. The mixture so obtained was extracted four times with 20 ml portions of chloroform. The extract was dried over anhydrous magnesium sulfate. The dried matter was then concentrated under reduced pressure. The residue was purified by chromatography on a silica gel column, whereby 383 mg of the title compound were obtained (yield: 95%).

後処理

  1. customthe mixture so obtained
  2. stirringwas then stirred for 10 minutes at room temperature
  3. customThe mixture so obtained
  4. extractionwas extracted four times with 20 ml portions of chloroform
  5. dry with materialThe extract was dried over anhydrous magnesium sulfate
  6. concentrationThe dried matter was then concentrated under reduced pressure
  7. customThe residue was purified by chromatography on a silica gel column

出典と根拠

ORDレコード
ord-1ffb27986c904f39a2c081fe5c161df6
出典データセット
uspto-grants-1997_09
特許番号
US05665888

関連ノート

読み込み中…