4-Nitro-1,2-phenylenediamine → HCID 3490719, compound
Reaction equation
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([NH2:10])=[C:6]([NH2:11])[CH:5]=1)([O-:3])=[O:2]>C(Cl)(Cl)Cl.CO>[CH2:9]([C:8]1[NH:11][C:6]2[CH:5]=[C:4]([N+:1]([O-:3])=[O:2])[CH:9]=[CH:8][C:7]=2[N:10]=1)[CH2:4][CH2:5][CH2:6][CH3:7]Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
Prepared from 4-nitrophenylenediamine in a manner similar to that of Example 4c. Yield: 78%; Rf (9/1 chloroform/methanol): 0.70; 1H-NMR (CDCl3) 10.2 (bs, 1H); 8.4 (d, J=1.5 Hz, 1H); 8.1 (dd, J=8.6 Hz, 1.53 Hz, 1H); 7.5 (d, J=8.6 Hz, 1H); 3.0 (t, 2H); 1.90 (m, 2H); 1.6-1.1 (m, 4H); 0.87 (t, 3H).
Sources & evidence
- ORD record
- ord-1d4d74e1b0d741fd9df5c673831710ff
- Source dataset
- uspto-grants-2010_03
- Patent number
- US07674809B2
Reaction notes
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