Ethanolamine → HCID 19090257, compound
Reaction equation
Cl[C:2]1[N:7]=[C:6]([NH:8][CH:9]2[CH2:14][C:13]([CH3:16])([CH3:15])[N:12]([O:17][CH:18]3[CH2:23][CH2:22][CH2:21][CH2:20][CH2:19]3)[C:11]([CH3:25])([CH3:24])[CH2:10]2)[N:5]=[C:4]([NH:26][CH:27]2[CH2:32][C:31]([CH3:34])([CH3:33])[N:30]([O:35][CH:36]3[CH2:41][CH2:40][CH2:39][CH2:38][CH2:37]3)[C:29]([CH3:43])([CH3:42])[CH2:28]2)[N:3]=1.[CH2:44]([CH2:46][NH2:47])[OH:45]>>[OH:45][CH2:44][CH2:46][NH:47][C:2]1[N:7]=[C:6]([NH:8][CH:9]2[CH2:14][C:13]([CH3:15])([CH3:16])[N:12]([O:17][CH:18]3[CH2:23][CH2:22][CH2:21][CH2:20][CH2:19]3)[C:11]([CH3:25])([CH3:24])[CH2:10]2)[N:5]=[C:4]([NH:26][CH:27]2[CH2:32][C:31]([CH3:33])([CH3:34])[N:30]([O:35][CH:36]3[CH2:37][CH2:38][CH2:39][CH2:40][CH2:41]3)[C:29]([CH3:43])([CH3:42])[CH2:28]2)[N:3]=1Participants
3
Procedure
The title compound is prepared from the reaction of 2-chloro-4,6-bis[(1-cyclohexyloxy-2,2,6,6-tetramethylpiperidin-4-yl)amino]-1,3,5-triazine with ethanolamine according to the procedure of Example 1.
Sources & evidence
- ORD record
- ord-7c1a7b56ce944d2a930d7cfc222c34e1
- Source dataset
- uspto-grants-1994_04
- Patent number
- US05300544
Reaction notes
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