Ethylenediamine → HCID 12763855, compound
Reaction equation
I.[CH3:2][CH:3]([CH3:17])[CH2:4][CH2:5][N:6]1[C:10]([NH:11][C:12](=[NH:15])SC)=[CH:9][C:8]([CH3:16])=[N:7]1.[CH2:18](N)[CH2:19][NH2:20]>C(O)CC>[CH3:2][CH:3]([CH3:17])[CH2:4][CH2:5][N:6]1[C:10]([NH:11][C:12]2[NH:20][CH2:19][CH2:18][N:15]=2)=[CH:9][C:8]([CH3:16])=[N:7]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
N[1-(3-methylbutyl)-3-methyl-5-pyrazolyl]-S-methyl isothiourea hydroiodide (29.0 g.) was suspended in 160 ml. n-propyl alcohol. Ethylene diamine (10.2 g.) was added and the solution was refluxed 18 hrs. The solvent was concentrated in vacuum and the residue was treated with KHCO3 in water. The resulting solid was recrystallized from CHCl3 -ether mixtures to obtain 14.3 g. product, mp 104°-106° C.
Workup
- temperaturethe solution was refluxed 18 hrs
- concentrationThe solvent was concentrated in vacuum
- additionthe residue was treated with KHCO3 in water
- customThe resulting solid was recrystallized from CHCl3 -ether mixtures
- customto obtain 14.3 g
Sources & evidence
- ORD record
- ord-eca0e808f1dd460ab75f81a0879d5e30
- Source dataset
- uspto-grants-1980_11
- Patent number
- US04234594
Reaction notes
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