O-Methylhydroxylamine hydrochloride → HCID 72448482, compound
Reaction equation
[NH2:1][C:2]1[C:11]2[N:12]=[C:13]([CH3:21])[N:14]([CH2:15][CH2:16][CH2:17][C:18](=O)[CH3:19])[C:10]=2[C:9]2[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=2[N:3]=1.Cl.[CH3:23][O:24][NH2:25]>>[CH3:23][O:24][N:25]=[C:18]([CH2:17][CH2:16][CH2:15][N:14]1[C:10]2[C:9]3[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=3[N:3]=[C:2]([NH2:1])[C:11]=2[N:12]=[C:13]1[CH3:21])[CH3:19]Participants
3
Procedure
By the general method described in Part F of Example 30, 5-(4-amino-2-methyl-1H-imidazo[4,5-c]quinolin-1-yl)pentan-2-one was reacted with O-methylhydroxylamine hydrochloride to provide 5-(4-amino-2-methyl-1H-imidazo[4,5-c]quinolin-1-yl)pentan-2-one O-methyloxime in about a 5.25 to 1 mixture of E and Z isomers as white needles after recrystallization from toluene, mp 158-161° C.
Sources & evidence
- ORD record
- ord-3756a961a8754114b26d0080e72d0bf6
- Source dataset
- uspto-grants-2014_07
- Patent number
- US08778963B2
Reaction notes
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