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2,5-Hexanedione → HCID 20294652, 화합물

HRID 1390007
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HRID 1390007 반응식
Cl.Cl.[NH:3]([C:5]1[N:6]=[N:7][C:8]([N:11]2[CH2:16][CH2:15][S:14][CH2:13][CH2:12]2)=[CH:9][CH:10]=1)[NH2:4].[CH3:17][C:18](=O)[CH2:19][CH2:20][C:21](=O)[CH3:22].C([O-])(=O)C.[Na+]>C(O)(=O)C>[CH3:22][C:21]1[N:4]([NH:3][C:5]2[N:6]=[N:7][C:8]([N:11]3[CH2:16][CH2:15][S:14][CH2:13][CH2:12]3)=[CH:9][CH:10]=2)[C:18]([CH3:17])=[CH:19][CH:20]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 80352,5-HexanedioneHCID 517045Sodium AcetateHCID 30439523(2H)-Pyridazinone, 6-(4-thiomorpholinyl)-, hydrazone, dihydrochloride

생성물 1

HCID 20294652HCID 20294652, 화합물수율 50%

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

3-Hydrazino-6-(4-thiomorpholinyl)-pyridazine di-hydrochloride and 2,5-hexanedione are reacted in acetic acid in the presence of sodium acetate according to the procedure of example 2. The product is recovered by evaporating the acetic acid and slurring the residue in aqueous sodium bicarbonate. The solid obtained after filtration is purified by chromatography through silicagel using a chloroform-methanol mixture 97.5:2.5 mixture as the eluent. Yield 50%. M.p. 203° C. (from ethyl acetate). Elemental analysis, I.R. and N.M.R. data are in agreement with the assigned structure.

후처리

  1. customThe product is recovered
  2. customby evaporating the acetic acid
  3. customThe solid obtained
  4. filtrationafter filtration
  5. customis purified by chromatography through silicagel

출처 및 근거

ORD 기록
ord-4a050224c583470b947e492d6e0a4c4e
출처 데이터셋
uspto-grants-1981_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04247551

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