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Hydrazine hydrate (1:1) → 6-Oxo-1-((2-(trimethylsilyl)ethoxy)methyl)-1,6-dihydropyridazine-4-carbohydrazide

HRID 500540
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HRID 500540 반응식
C([O:3][C:4]([C:6]1[CH:7]=[N:8][N:9]([CH2:13][O:14][CH2:15][CH2:16][Si:17]([CH3:20])([CH3:19])[CH3:18])[C:10](=[O:12])[CH:11]=1)=O)C.O.[NH2:22][NH2:23]>C(O)C>[O:12]=[C:10]1[N:9]([CH2:13][O:14][CH2:15][CH2:16][Si:17]([CH3:20])([CH3:19])[CH3:18])[N:8]=[CH:7][C:6]([C:4]([NH:22][NH2:23])=[O:3])=[CH:11]1
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참가 물질

4

반응물 2

HCID 24654Hydrazine hydrate (1:1)HCID 248517026-Oxo-1-(2-trimethylsilanyl-ethoxymethyl)-1,6-dihydro-pyridazine-4-carboxylic acid ethyl ester

생성물 1

HCID 248517036-Oxo-1-((2-(trimethylsilyl)ethoxy)methyl)-1,6-dihydropyridazine-4-carbohydrazide

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
50 °C

실험 절차

The title compound from Example 19.2 (0.85 g, 2.8 mmol) was stirred in ethanol. Hydrazine hydrate (0.720 g, 14.2 mmol) was added to the solution and the reaction was stirred at 50° C. for 1 hour. The reaction was concentrated and triturated with methanol and diethyl ether to produce a precipitate which was collected by vacuum filtration as the title compound (0.56 g, 57%).

후처리

  1. concentrationThe reaction was concentrated
  2. customtriturated with methanol and diethyl ether
  3. customto produce a precipitate which
  4. filtrationwas collected by vacuum filtration as the title compound (0.56 g, 57%)

출처 및 근거

ORD 기록
ord-a7cd0a8d955c472eaf3c100b1e724384
출처 데이터셋
uspto-grants-2010_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07772235B2

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