홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Hydrazine hydrate (1:1) → HCID 16641866, 화합물

HRID 1023529
노트
인쇄 미리보기

반응식

HRID 1023529 반응식
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[CH:4][C:3]=1[O:9][C:10]1[CH:15]=[CH:14][C:13]([N+:16]([O-])=O)=[CH:12][N:11]=1.O.NN>C(O)C.[Pd]>[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[CH:4][C:3]=1[O:9][C:10]1[N:11]=[CH:12][C:13]([NH2:16])=[CH:14][CH:15]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 24654Hydrazine hydrate (1:1)HCID 24623396HCID 24623396, 화합물2회

생성물 1

HCID 16641866HCID 16641866, 화합물수율 88.2%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 702Ethanol용매

실험 절차

2-[(2,5-dimethylphenyl)oxy]-5-nitropyridine (Intermediate 33, 140 mg, 0.450 mmol) was dissolved in ethanol (3 mL). Hydrazine hydrate (83 μL, 0.884 mmol) and palladium on carbon (47 mg, 0.044 mmol) were added. The reaction mixture was heated at reflux under argon. After overnight heating, the reaction was cooled down. The reaction mixture was filtered. The organic phase was evaporated under vacuum. The residue was purified by SCX (wash with MeOH, desorbed with 2N methanolic ammonia). Evaporation afforded the title compound (85 mg).

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

후처리

  1. temperatureThe reaction mixture was heated
  2. temperatureat reflux under argon
  3. temperatureAfter overnight heating
  4. temperaturethe reaction was cooled down
  5. filtrationThe reaction mixture was filtered
  6. customThe organic phase was evaporated under vacuum
  7. customThe residue was purified by SCX (wash with MeOH, desorbed with 2N methanolic ammonia)
  8. customEvaporation

출처 및 근거

ORD 기록
ord-15e424a75c92465cac059aff32d64a8c
출처 데이터셋
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08722695B2

반응 노트

불러오는 중…