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Hydrazinecarboxaldehyde → 3-(4-nitrophenyl)-1H-1,2,4-triazole

HRID 1807198
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HRID 1807198 반응식
Cl.CO[C:4](=[NH:14])[C:5]1[CH:10]=[CH:9][C:8]([N+:11]([O-:13])=[O:12])=[CH:7][CH:6]=1.[CH:15]([NH:17][NH2:18])=O>N1C=CC=CC=1>[N+:11]([C:8]1[CH:7]=[CH:6][C:5]([C:4]2[NH:18][N:17]=[CH:15][N:14]=2)=[CH:10][CH:9]=1)([O-:13])=[O:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 12229HydrazinecarboxaldehydeHCID 12410479HCID 12410479, 화합물

생성물 1

HCID 28252243-(4-nitrophenyl)-1H-1,2,4-triazole

시약·촉매·용매 1

HCID 1049Pyridine용매

실험 절차

4-Nitro-benzimidic acid methyl ester hydrochloride (635 mg, 2.93 mmol) was suspended in pyridine (7 mL) and formic hydrazide (Aldrich, 178 mg, 2.95 mmol) was added and the mixture was stirred at rt for 1 hr. The solvent was removed and the residue was dissolved in toluene (10 mL) and the mixture was stirred at reflux for 1.5 hrs. the mixture was cooled and water was added. The organic layer was separated and dried over sodium sulfate. The solvent was removed and the residue was suspended in 25% EtOAc/Hexanes and the solid was filtered to give a solid. 510 mg.

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  1. customThe solvent was removed
  2. dissolutionthe residue was dissolved in toluene (10 mL)
  3. stirringthe mixture was stirred
  4. temperatureat reflux for 1.5 hrs
  5. temperaturethe mixture was cooled
  6. additionwater was added
  7. customThe organic layer was separated
  8. dry with materialdried over sodium sulfate
  9. customThe solvent was removed
  10. filtrationthe solid was filtered
  11. customto give a solid

출처 및 근거

ORD 기록
ord-e9d962c9286948cbac36aa0a6d7abc96
출처 데이터셋
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08354444B2

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