Cyclohexylamine → 3-Hydroxy-6-methoxy-N-cyclohexylpicolinamide
Reaction equation
C(OC1C(C(O)=O)=NC=CC=1OC)C1C=CC=CC=1.C([O:27][C:28]1[C:29]([C:36]([OH:38])=O)=[N:30][C:31]([O:34][CH3:35])=[CH:32][CH:33]=1)C1C=CC=CC=1.COC1C=CC(O[C:46]2[CH:52]=[CH:51][C:49]([NH2:50])=[CH:48][CH:47]=2)=CC=1.C1(N)CCCCC1>>[OH:27][C:28]1[C:29]([C:36]([NH:50][CH:49]2[CH2:51][CH2:52][CH2:46][CH2:47][CH2:48]2)=[O:38])=[N:30][C:31]([O:34][CH3:35])=[CH:32][CH:33]=1Participants
5
Procedure
The procedure of Example 29 was repeated, except that 3-benzyloxy-4-methoxypicolinic acid was changed to 3-benzyloxy-6-methoxypicolinic acid and 4-(4′-methoxyphenoxy)aniline was changed to cyclohexylamine. Thus, the title compound was prepared.
Sources & evidence
- ORD record
- ord-8d1f4b659e7c40c79de9bc002ed22584
- Source dataset
- uspto-grants-2007_02
- Patent number
- US07183278B1
Reaction notes
Loading…