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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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2-Aminothiophenol → 1,3-Benzenediol, 5-(2-benzothiazolyl)-

HRID 338782
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HRID 338782 반응식
C([O-])(=O)C.[Na+].[OH:6][C:7]1[CH:8]=[C:9]([CH:12]=[C:13]([OH:15])[CH:14]=1)[CH:10]=O.[NH2:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=1[SH:23]>C(O)(=O)C>[S:23]1[C:18]2[CH:19]=[CH:20][CH:21]=[CH:22][C:17]=2[N:16]=[C:10]1[C:9]1[CH:12]=[C:13]([OH:15])[CH:14]=[C:7]([OH:6])[CH:8]=1
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참가 물질

5

반응물 3

HCID 87132-AminothiophenolHCID 943653,5-DihydroxybenzaldehydeHCID 517045Sodium Acetate

생성물 1

HCID 682793671,3-Benzenediol, 5-(2-benzothiazolyl)-수율 48.8%

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

An acetic acid (0.8 mL) and sodium acetate (196.6 mg, 2.40 mmol) were added to a suspension including 3,5-dihydroxybenzaldehyde (91.6 mg, 0.66 mmol) and 2-aminothiophenol (0.095 mL, 0.80 mmol, purity: 90%), and then, the reaction mixture was refluxed for 2 hours. The resultant precipitate was filtered, and the filtered product was washed with water and methylene chloride to obtain a gray solid Compound 21 (78.3 mg, 48.6%).

후처리

  1. temperaturethe reaction mixture was refluxed for 2 hours
  2. filtrationThe resultant precipitate was filtered
  3. washthe filtered product was washed with water and methylene chloride

출처 및 근거

ORD 기록
ord-867faa4d77614f7dbf1ca34fca4ac2a0
출처 데이터셋
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08889881B2

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