Beta-Alanine → HCID 54311176, compound
Reaction equation
Cl[C:2]1[N:7]=[C:6]([NH:8][CH2:9][CH2:10][CH2:11][CH2:12][CH:13]2[CH2:18][C:17]([CH3:20])([CH3:19])[N:16]([O:21][CH3:22])[C:15]([CH3:24])([CH3:23])[CH2:14]2)[N:5]=[C:4]([NH:25][CH2:26][CH2:27][CH2:28][CH2:29][CH:30]2[CH2:35][C:34]([CH3:37])([CH3:36])[N:33]([O:38][CH3:39])[C:32]([CH3:41])([CH3:40])[CH2:31]2)[N:3]=1.[NH2:42][CH2:43][CH2:44][C:45]([OH:47])=[O:46]>>[CH3:39][O:38][N:33]1[C:32]([CH3:41])([CH3:40])[CH2:31][CH:30]([CH2:29][CH2:28][CH2:27][CH2:26][NH:25][C:4]2[N:5]=[C:6]([NH:8][CH2:9][CH2:10][CH2:11][CH2:12][CH:13]3[CH2:18][C:17]([CH3:20])([CH3:19])[N:16]([O:21][CH3:22])[C:15]([CH3:24])([CH3:23])[CH2:14]3)[N:7]=[C:2]([NH:42][CH2:43][CH2:44][C:45]([OH:47])=[O:46])[N:3]=2)[CH2:35][C:34]1([CH3:37])[CH3:36]Participants
3
Procedure
The title compound is prepared from the reaction of 2-chloro-4,6-bis[N-(1-methoxy-2,2,6,6-tetramethylpiperidin-4-yl)butylamino]-1,3,5-triazine and β-alanine according to the procedure of Example 15.
Sources & evidence
- ORD record
- ord-637e81638d2b4e7d9a082516606fd0a0
- Source dataset
- uspto-grants-1994_04
- Patent number
- US05300544
Reaction notes
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