Methoxyisopropylamine → HCID 18362814, compound
Reaction equation
[CH2:1]([NH:3][C:4]1[C:5]([N:10]2[CH2:15][CH2:14][N:13]([C:16]([C:18]3[CH:26]=[CH:25][C:21]([C:22]([OH:24])=O)=[CH:20][N:19]=3)=[O:17])[CH2:12][CH2:11]2)=[N:6][CH:7]=[CH:8][CH:9]=1)[CH3:2].[CH3:27][CH:28]([NH2:32])[CH2:29][O:30][CH3:31]>>[CH2:1]([NH:3][C:4]1[C:5]([N:10]2[CH2:11][CH2:12][N:13]([C:16]([C:18]3[CH:26]=[CH:25][C:21]([C:22](=[O:24])[NH:32][CH:28]([CH3:27])[CH2:29][O:30][CH3:31])=[CH:20][N:19]=3)=[O:17])[CH2:14][CH2:15]2)=[N:6][CH:7]=[CH:8][CH:9]=1)[CH3:2]Participants
3
Procedure
By the same procedure as described in the example 24, the synthesis was carried out starting with 6-[1-[3-(ethylamino)-2-pyridyl]piperazin-4-yl-carbonyl]nicotinic acid and using 2-methoxyisopropylamine. And then, the product was recrystallized with isopropanol and hexane to give a desired compound.
Workup
- customAnd then, the product was recrystallized with isopropanol and hexane
Sources & evidence
- ORD record
- ord-eeadbc2d0106485a9af1a454f45f4b6c