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Benzoyl chloride → 5-(4-Benzoylaminophenyl)thiazolidine-2,4-dione

HRID 1742824
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HRID 1742824 반응식
O1CCOCC1.[NH2:7][C:8]1[CH:13]=[CH:12][C:11]([CH:14]2[S:18][C:17](=[O:19])[NH:16][C:15]2=[O:20])=[CH:10][CH:9]=1.[C:21](Cl)(=[O:28])[C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1>C(N(CC)CC)C>[C:21]([NH:7][C:8]1[CH:9]=[CH:10][C:11]([CH:14]2[S:18][C:17](=[O:19])[NH:16][C:15]2=[O:20])=[CH:12][CH:13]=1)(=[O:28])[C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7412Benzoyl chlorideHCID 312751,4-DioxaneHCID 128509725-(4-Aminophenyl)thiazolidine-2,4-dione

생성물 1

HCID 190060595-(4-Benzoylaminophenyl)thiazolidine-2,4-dione수율 93.3%

시약·촉매·용매 1

HCID 8471Triethylamine용매

실험 절차

Into 20 ml of dioxane were dissolved 0.5 g of 5-(4-aminophenyl) thiazolidine-2,4-dione, and, after added 0.34 g of benzoyl chloride and further added dropwise 0.24 g of triethylamine, the mixture was refluxed for 1 hour. After cooling by standing, the reaction mixture was poured into 150 ml of ice water and the crystals deposited were collected by filtration, washed with water and dried. These were recrystallized from chloroform to obtain 0.70 g of title compound.

후처리

  1. temperaturethe mixture was refluxed for 1 hour
  2. temperatureAfter cooling
  3. filtrationthe crystals deposited were collected by filtration
  4. washwashed with water
  5. customdried
  6. customThese were recrystallized from chloroform

출처 및 근거

ORD 기록
ord-9beb242176cd4c92aac25d7e1e4edc8e
출처 데이터셋
uspto-grants-1994_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05342850

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