Sodium Acetate → 5-[[7-[(5-Ethyl-2-pyridinyl)methoxy]quinolin-3-yl]methyl]-2-imino-1,3-thiazolidin-4-one

HRID 1938346노트

반응식

HRID 1938346 반응식
Br[CH:2]([CH2:7][C:8]1[CH:9]=[N:10][C:11]2[C:16]([CH:17]=1)=[CH:15][CH:14]=[C:13]([O:18][CH2:19][C:20]1[CH:25]=[CH:24][C:23]([CH2:26][CH3:27])=[CH:22][N:21]=1)[CH:12]=2)[C:3]([O:5]C)=O.[NH2:28][C:29]([NH2:31])=[S:30].C([O-])(=O)C.[Na+]>C(O)C>[CH2:26]([C:23]1[CH:24]=[CH:25][C:20]([CH2:19][O:18][C:13]2[CH:12]=[C:11]3[C:16]([CH:17]=[C:8]([CH2:7][CH:2]4[S:30][C:29](=[NH:28])[NH:31][C:3]4=[O:5])[CH:9]=[N:10]3)=[CH:15][CH:14]=2)=[N:21][CH:22]=1)[CH3:27]

참가 물질

5

실험 절차

In ethanol (20 mL) was dissolved the crude residue (790 mg) of methyl 2-bromo-3-[7-(5-ethyl-2-pyridylmethoxy)-3-quinolyl]propionate. The solution was heated under reflux for 15 hours after addition of thiourea (140 mg, 1.84 mmol.) and sodium acetate (150 mg, 1.84 mmol.). After the completion of reaction was confirmed, ethanol was distilled off. To the residue were added ethyl acetate and aqueous sodium hydrogen carbonate. The organic portion was recovered, washed with water, and dried over sodium sulfate.

후처리

  1. temperatureThe solution was heated
  2. temperatureunder reflux for 15 hours
  3. customAfter the completion of reaction
  4. distillationethanol was distilled off
  5. additionTo the residue were added ethyl acetate and aqueous sodium hydrogen carbonate
  6. customThe organic portion was recovered
  7. washwashed with water
  8. dry with materialdried over sodium sulfate

출처 및 근거

ORD 기록
ord-b4c2325227fb431a821ce6554d1a385d
출처 데이터셋
uspto-grants-1997_12
특허 번호
US05693651

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