Hydrochloric Acid → HCID 21272622, compound
Reaction equation
[C:1]([C:3]1[N:4]([CH2:8][C:9]2[CH:13]=[CH:12][O:11][CH:10]=2)[CH:5]=[CH:6][N:7]=1)#[N:2].Cl>[Pd].C(O)C>[NH2:2][CH2:1][C:3]1[N:4]([CH2:8][C:9]2[CH:13]=[CH:12][O:11][CH:10]=2)[CH:5]=[CH:6][N:7]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
Place 4.0 g (0.021 mol) 2-cyano-1-(3-furylmethyl)-1H-imidazole, 20 ml ethanolic HCl, 20 ml ethanol and 1 g 10% Pd/C in a Parr hydrogenator with an initial pressure of 52 psi. After 18 hours remove the reaction mixture from the Parr hydrogenator, add 20 ml H2O, remove the catalyst by filtration, concentrate the filtrate to obtain an off-white solid which is recrystallized from ethanol containing a little concentrated HCl to give the desired product as a white solid.
Workup
- customAfter 18 hours remove the reaction mixture from the Parr hydrogenator
- additionadd 20 ml H2O
- customremove the catalyst
- filtrationby filtration
- concentrationconcentrate the filtrate
- customto obtain an off-white solid which
- customis recrystallized from ethanol containing a little concentrated HCl
Sources & evidence
- ORD record
- ord-6c0325f14d2b48079460410540d27d47
- Source dataset
- uspto-grants-1989_03
- Patent number
- US04810800
Reaction notes
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