2-(Diethylamino)-6-methylisonicotinic acid → HCID 68579414, compound
Reaction equation
[OH:1][NH:2][C:3]([C:5]1[CH:10]=[CH:9][C:8]([CH2:11][C:12]([OH:14])=[O:13])=[CH:7][CH:6]=1)=[NH:4].[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]>>[CH2:28]([N:17]([CH2:15][CH3:16])[C:18]1[CH:19]=[C:20]([C:21]2[O:1][N:2]=[C:3]([C:5]3[CH:6]=[CH:7][C:8]([CH2:11][C:12]([OH:14])=[O:13])=[CH:9][CH:10]=3)[N:4]=2)[CH:24]=[C:25]([CH3:27])[N:26]=1)[CH3:29]Participants
3
Procedure
The title compound is prepared in analogy to Example 5 starting from [4-(N-hydroxycarbamimidoyl)-phenyl]-acetic acid and 2-diethylamino-6-methyl-isonicotinic acid; LC-MS: tR=0.78 min; [M+1]+=367.13.
Sources & evidence
- ORD record
- ord-98fbddaba2b14f969ec3733435ff8ea6
- Source dataset
- uspto-grants-2013_11
- Patent number
- US08592460B2
Reaction notes
Loading…