Ethanolamine → HCID 54511849, compound

HRID 1463724Notes

Reaction equation

HRID 1463724 reaction equation
Cl[C:2]1[N:7]=[C:6]([NH:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH:21]2[CH2:26][C:25]([CH3:28])([CH3:27])[N:24]([O:29][CH:30]3[CH2:35][CH2:34][CH2:33][CH2:32][CH2:31]3)[C:23]([CH3:37])([CH3:36])[CH2:22]2)[N:5]=[C:4]([NH:38][CH2:39][CH2:40][CH2:41][CH2:42][CH2:43][CH2:44][CH2:45][CH2:46][CH2:47][CH2:48][CH2:49][CH2:50][CH:51]2[CH2:56][C:55]([CH3:58])([CH3:57])[N:54]([O:59][CH:60]3[CH2:65][CH2:64][CH2:63][CH2:62][CH2:61]3)[C:53]([CH3:67])([CH3:66])[CH2:52]2)[N:3]=1.[CH2:68]([CH2:70][NH2:71])[OH:69]>>[OH:69][CH2:68][CH2:70][NH:71][C:2]1[N:7]=[C:6]([NH:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH:21]2[CH2:26][C:25]([CH3:28])([CH3:27])[N:24]([O:29][CH:30]3[CH2:31][CH2:32][CH2:33][CH2:34][CH2:35]3)[C:23]([CH3:37])([CH3:36])[CH2:22]2)[N:5]=[C:4]([NH:38][CH2:39][CH2:40][CH2:41][CH2:42][CH2:43][CH2:44][CH2:45][CH2:46][CH2:47][CH2:48][CH2:49][CH2:50][CH:51]2[CH2:56][C:55]([CH3:57])([CH3:58])[N:54]([O:59][CH:60]3[CH2:61][CH2:62][CH2:63][CH2:64][CH2:65]3)[C:53]([CH3:67])([CH3:66])[CH2:52]2)[N:3]=1

Participants

3

Reactant 2

HCID 700EthanolamineHCID 54139715HCID 54139715, compound

Product 1

HCID 54511849HCID 54511849, compound

Procedure

The title compound is prepared from the reaction of 2-chloro-4,6-bis[N-(1-cyclohexyloxy-2,2,6,6-tetramethylpiperidin-4-yl)dodecylamino]-1,3,5-triazine with ethanolamine according to the procedure of Example 1.

Sources & evidence

ORD record
ord-f7f4da85e27b44e889ce2837e3da125a
Source dataset
uspto-grants-1994_04
Patent number
US05300544

Reaction notes

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