Acetone → HCID 58835304, compound
Reaction equation
[NH2:1][O:2][CH2:3][CH2:4][CH2:5][CH2:6][N:7]1[C:19]2[C:18]3[CH2:17][CH2:16][CH2:15][CH2:14][C:13]=3[N:12]=[C:11]([NH2:20])[C:10]=2[N:9]=[C:8]1[CH2:21][O:22][CH2:23][CH3:24].[CH3:25][C:26]([CH3:28])=O>>[NH2:20][C:11]1[C:10]2[N:9]=[C:8]([CH2:21][O:22][CH2:23][CH3:24])[N:7]([CH2:6][CH2:5][CH2:4][CH2:3][O:2][N:1]=[C:26]([CH3:28])[CH3:25])[C:19]=2[C:18]2[CH2:17][CH2:16][CH2:15][CH2:14][C:13]=2[N:12]=1Participants
3
Procedure
The method described in Example 3 can be used to treat 1-[4-(aminooxy)butyl]-2-(ethoxymethyl)-6,7,8,9-tetrahydro-1H-imidazo[4,5-c]quinolin-4-amine with acetone to provide acetone O-{4-[4-amino-2-(ethoxymethyl)-6,7,8,9-tetrahydro-1H-imidazo[4,5-c]quinolin-1-yl]butyl}oxime.
Sources & evidence
- ORD record
- ord-0da3811383254430a92d8a165655b6c5
- Source dataset
- uspto-grants-2014_03
- Patent number
- US08673932B2
Reaction notes
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