Cyclohexylamine → N-cyclohexyl-5-methyl-7-phenylimidazo[5,1-f][1,2,4]triazin-2-amine
Reaction equation
[CH3:1][C:2]1[N:3]=[C:4]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[N:5]2[C:10]=1[CH:9]=[N:8][C:7](SC)=[N:6]2.CC1N=C(C2C=CC=CC=2)N2C=1C=NC(S(C)(=O)=O)=N2.[CH:39]1([NH2:45])[CH2:44][CH2:43][CH2:42][CH2:41][CH2:40]1>C(O)C>[CH:39]1([NH:45][C:7]2[N:8]=[CH:9][C:10]3=[C:2]([CH3:1])[N:3]=[C:4]([C:13]4[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=4)[N:5]3[N:6]=2)[CH2:44][CH2:43][CH2:42][CH2:41][CH2:40]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Applying the displacement procedure, using 5-methyl-2-(methylthio)-7-phenylimidazo[5,1-f][1,2,4]triazine (Intermediate 72) (50 mg, 0.17 mmol), cyclohexylamine (0.02 mL, 0.17 mmol) and ethanol (2.5 mL) to afford N-cyclohexyl-5-methyl-7-phenylimidazo[5,1-f][1,2,4]triazin-2-amine (8 mg) as a yellow solid. MS m/z 308 (M+1).
Sources & evidence
- ORD record
- ord-30dadda79ab84e9185edbc6cd457d955
- Source dataset
- uspto-grants-2008_12
- Patent number
- US07462614B2
Reaction notes
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