Ethylenediamine → HCID 21409985, compound

HRID 2071944Notes

Reaction equation

HRID 2071944 reaction equation
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([N:16]([CH2:18][CH2:19]Cl)[CH3:17])=[C:6]([CH:15]=1)[C:7]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)=O.[CH2:21]([NH2:24])[CH2:22][NH2:23].C(N(CC)CC)C>C(O)C>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[N:16]([CH3:17])[CH2:18][CH2:19][N:23]3[CH2:22][CH2:21][NH:24][C:7]3([C:9]3[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=3)[C:6]=2[CH:15]=1

Participants

5

Reactant 3

HCID 3301EthylenediamineHCID 8471TriethylamineHCID 21823034HCID 21823034, compound

Product 1

HCID 21409985HCID 21409985, compound

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

A solution of 5.0 g. (16 mmole) of 5-chloro-2-(2-chloroethylmethylamino)benzophenone, 3.0 g. (50 mmole) of ethylenediamine, 50 ml. of triethylamine and 250 ml. of ethanol was stirred at reflux for 48 hours. The solvents were removed by evaporation and the residue containing starting material and the product was washed with water, chromatographed over Florisil, and recrystallized from petroleum ether to give the above-titled product as yellow prisms, m.p. 100°-102°.

Workup

  1. temperatureat reflux for 48 hours
  2. customThe solvents were removed by evaporation
  3. additionthe residue containing
  4. washthe product was washed with water
  5. customchromatographed over Florisil
  6. customrecrystallized from petroleum ether

Sources & evidence

ORD record
ord-3fadf1fd0cca4eab817c651b7f048561
Source dataset
uspto-grants-1977_09
Patent number
US04049667

Reaction notes

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