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

HRID 1377950노트

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HRID 1377950 반응식
[NH2:1][C:2]1[S:3][CH:4]=[C:5](/[C:7](=[N:11]/[O:12][CH3:13])/[C:8]([OH:10])=[O:9])[N:6]=1.[CH3:14][N:15]([CH3:18])[CH:16]=O.P(Cl)(Cl)(Cl)=O.[OH-].[Na+].O1CCC[CH2:27]1>CO>[CH3:14][N:15]([CH:18]=[N:1][C:2]1[S:3][CH:4]=[C:5](/[C:7](=[N:11]/[O:12][CH3:13])/[C:8]([O:10][CH3:27])=[O:9])[N:6]=1)[CH3:16]

참가 물질

7

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온도
5 °C

실험 절차

(Z)-2-(2-aminothiazol-4-yl)-2-methoxyiminoacetic acid (0.5 g, 2.5 mmol) was dissolved in 20 ml of tetrahydrofuran. Subsequent to the addition of 0.72 g (9.9 mmol) of dimethylformamide, the resulting solution was cooled to 5° C. The solution was added with 1.52 g (9.9 mmol) of phosphorus oxychloride and the resulting mixture was stirred for 3 hours. Methanol (20 ml) was added to the reaction mixture, followed by stirring for 10 minutes. A 2N aqueous solution of sodium hydroxide was added to the reaction mixture to adjust its pH to 7. The reaction mixture so obtained was extracted three times with 100 ml portions of chloroform. The organic phases were combined and then dried. The solvent was distilled off under reduced pressure. The residue was purified by chromatography on a silica gel column, whereby 0.63 g of the title compound was obtained (yield: 94%).

후처리

  1. stirringby stirring for 10 minutes
  2. customThe reaction mixture so obtained
  3. extractionwas extracted three times with 100 ml portions of chloroform
  4. customdried
  5. distillationThe solvent was distilled off under reduced pressure
  6. customThe residue was purified by chromatography on a silica gel column

출처 및 근거

ORD 기록
ord-45376663b3b1453e9a478de5a12b859b
출처 데이터셋
uspto-grants-1997_09
특허 번호
US05665888

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