Diethanolamine → HCID 53898869, 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.[NH:42]([CH2:46][CH2:47][OH:48])[CH2:43][CH2:44][OH:45]>>[OH:45][CH2:44][CH2:43][N:42]([CH2:46][CH2:47][OH:48])[C:2]1[N:3]=[C:4]([NH:25][CH2:26][CH2:27][CH2:28][CH2:29][CH:30]2[CH2:35][C:34]([CH3:36])([CH3:37])[N:33]([O:38][CH3:39])[C:32]([CH3:40])([CH3:41])[CH2:31]2)[N:5]=[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]([CH3:23])([CH3:24])[CH2:14]2)[N:7]=1Participants
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 diethanolamine according to the procedure of Example 1.
Sources & evidence
- ORD record
- ord-ff048da856c142708b2a1639f2d7bba5
- Source dataset
- uspto-grants-1994_04
- Patent number
- US05300544
Reaction notes
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