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

HRID 266250

반응식

HRID 266250 반응식
[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]

참가 물질

6

실험 절차

Dimethylaminochloromethyleneammonium chloride (400 mg, 3.1 mmol) was dissolved in 10 ml of tetrahydrofuran. Added to the resulting solution were 300 mg of (Z)-2-(2-aminothiazol-4-yl)-2-methoxyimino-acetic acid, followed by stirring at room temperature for 16 hours. Methanol (10 ml ) was added thereto. The mixture so obtained was stirred For 10 minutes at room temperature. The mixture was then 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 gelcolumn, whereby 293 mg of the title compound were obtained (yield: 72%).

후처리

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

출처 및 근거

ORD 기록
ord-944525dab3194ffb8e21fae15c10afd5
출처 데이터셋
uspto-grants-1997_07
특허 번호
US05650518

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