Ethylenediamine → N1-(pyridin-4-yl)ethane-1,2-diamine

HRID 1393154

Reaction equation

HRID 1393154 reaction equation
[CH2:1]([NH2:4])[CH2:2][NH2:3].Cl.Br[C:7]1[CH:12]=[CH:11][N:10]=[CH:9][CH:8]=1.C(=O)([O-])[O-].[K+].[K+]>>[N:10]1[CH:11]=[CH:12][C:7]([NH:3][CH2:2][CH2:1][NH2:4])=[CH:8][CH:9]=1

Participants

4

Procedure

Ethylenediamine (10.4 ml, 155 mmol) was added to 4-bromopyridine hydrochloride (3.00 g, 15.5 mmol) under a nitrogen atmosphere, and the mixture was refluxed for 1.5 hours. The temperature was cooled to room temperature, potassium carbonate (8.57 g, 62.0 mmol) was added to the reaction mixture, and the whole was stirred for 10 minutes. Then, the solid was filtered out and washed with toluene and 2-propanol successively. The filtrate was concentrated under reduced pressure, the residue was purified by basic silica gel column chromatography, and the resulting solid was filtered off with diisopropyl ether to give 1.63 g (77%) of the titled compound as a pale yellow solid.

Workup

  1. temperaturethe mixture was refluxed for 1.5 hours
  2. filtrationThen, the solid was filtered out
  3. washwashed with toluene and 2-propanol successively
  4. concentrationThe filtrate was concentrated under reduced pressure
  5. customthe residue was purified by basic silica gel column chromatography
  6. filtrationthe resulting solid was filtered off with diisopropyl ether

Sources & evidence

ORD record
ord-f833b4e0a0284d34885a5193506acd8e
Source dataset
uspto-grants-2008_03
Patent number
US07345064B2

Linked notes

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