2-(Diethylamino)-6-methylisonicotinic acid → HCID 68577894, compound
Reaction equation
[OH:1][NH:2][C:3](=[NH:14])[C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([O:10][CH3:11])[C:5]=1[O:12][CH3:13].[CH2:15]([N:17]([CH2:28][CH3:29])[C:18]1[CH:19]=[C:20]([CH:24]=[C:25]([CH3:27])[N:26]=1)[C:21](O)=O)[CH3:16]>>[CH3:13][O:12][C:5]1[C:6]([O:10][CH3:11])=[CH:7][CH:8]=[CH:9][C:4]=1[C:3]1[N:14]=[C:21]([C:20]2[CH:24]=[C:25]([CH3:27])[N:26]=[C:18]([N:17]([CH2:28][CH3:29])[CH2:15][CH3:16])[CH:19]=2)[O:1][N:2]=1Participants
3
Procedure
The title compound is prepared in analogy to Example 5 starting from N-hydroxy-2,3-dimethoxy-benzamidine and 2-diethylamino-6-methyl-isonicotinic acid; LC-MS: tR=1.16*min; [M+1]+=369.03.
Sources & evidence
- ORD record
- ord-e39ad0c1b28b4574af95e8c57e96dcda
- Source dataset
- uspto-grants-2013_11
- Patent number
- US08592460B2
Reaction notes
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