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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Thiazolidinedione → 2,4-Thiazolidinedione, 5-(2-thienylmethylene)-, (Z)-

HRID 6171
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HRID 6171 반응식
[S:1]1[CH2:5][C:4](=[O:6])[NH:3][C:2]1=[O:7].[S:8]1[CH:12]=[CH:11][CH:10]=[C:9]1[CH:13]=O.N1CCCCC1>C(O)C>[S:8]1[CH:12]=[CH:11][CH:10]=[C:9]1[CH:13]=[C:5]1[S:1][C:2](=[O:7])[NH:3][C:4]1=[O:6]
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참가 물질

5

반응물 3

HCID 5437ThiazolidinedioneHCID 73642-ThiophenecarboxaldehydeHCID 8082Piperidine

생성물 1

HCID 36416932,4-Thiazolidinedione, 5-(2-thienylmethylene)-, (Z)-수율 66.6%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a solution of 20 g (171 mmol) of 2,4-thiazolidinedione and 16.0 ml (171 mmol) of 2-thiophenecarboxaldehyde in 350 ml of ethanol, 1.68 ml (17.1 mmol) of piperidine was added, and the mixture was heated under reflux for 5 hours. After cooling, the precipitated crystals were filtered and washed with cooled ethanol to give 24.03 g of the desired compound (66.6% yield, pale yellow crystals).

후처리

  1. temperaturethe mixture was heated
  2. temperatureunder reflux for 5 hours
  3. temperatureAfter cooling
  4. filtrationthe precipitated crystals were filtered
  5. washwashed with cooled ethanol

출처 및 근거

ORD 기록
ord-fe71a2c02edc41da90a957171964ea9f
출처 데이터셋
uspto-grants-1993_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05246948

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