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Ethylenediamine → N-[1-(1-methyl-1H-pyrazol-4-yl)ethyl]ethane-1,2-diamine

HRID 420850
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반응식

HRID 420850 반응식
[CH3:1][N:2]1[CH:6]=[C:5]([C:7](=O)[CH3:8])[CH:4]=[N:3]1.[CH2:10]([NH2:13])[CH2:11][NH2:12].C([BH3-])#N.[Na+].C(=O)([O-])O.[Na+]>CO.O1CCCC1.C(O)(=O)C>[CH3:1][N:2]1[CH:6]=[C:5]([CH:7]([NH:12][CH2:11][CH2:10][NH2:13])[CH3:8])[CH:4]=[N:3]1
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참가 물질

8

반응물 4

HCID 3301EthylenediamineHCID 516892Sodium BicarbonateHCID 35969391-(1-methyl-1H-pyrazol-4-yl)ethan-1-oneHCID 5003444Sodium cyanoborohydride

생성물 1

HCID 14009898N-[1-(1-methyl-1H-pyrazol-4-yl)ethyl]ethane-1,2-diamine수율 48.1%

시약·촉매·용매 3

HCID 176
Acetic Acid
용매
HCID 887Methanol용매
HCID 8028Tetrahydrofuran용매

실험 절차

1-(1-Methyl-1H-pyrazol-4-yl)-ethanone (250 mg) and ethylenediamine (362 mg) were dissolved in methanol (10 ml), the solution was added with acetic acid (1.21 g) and sodium cyanoborohydride (189 mg), and the mixture was stirred at room temperature for 48 hours. The reaction mixture was added with saturated aqueous sodium hydrogencarbonate and tetrahydrofuran, the layers were separated, and then the organic layer was dried over anhydrous magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure, and the resulting residue was purified by silica gel column chromatography (chloroform:methanol:28% aqueous ammonia=10:1:0.1) to obtain the title compound (163 mg).

후처리

  1. customthe layers were separated
  2. dry with materialthe organic layer was dried over anhydrous magnesium sulfate
  3. filtrationfiltered
  4. concentrationThe filtrate was concentrated under reduced pressure
  5. customthe resulting residue was purified by silica gel column chromatography (chloroform:methanol:28% aqueous ammonia=10:1:0.1)

출처 및 근거

ORD 기록
ord-c448b2dc18304b66a020f37dce9cbb5a
출처 데이터셋
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08097708B2

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