Ethanolamine → HCID 54521421, compound

HRID 1463721Notes

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][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH3:39])[C:15]([CH3:41])([CH3:40])[CH2:14]2)[N:5]=[C:4]([NH:42][CH2:43][CH2:44][CH2:45][CH2:46][CH:47]2[CH2:52][C:51]([CH3:54])([CH3:53])[N:50]([O:55][CH2:56][CH2:57][CH2:58][CH2:59][CH2:60][CH2:61][CH2:62][CH2:63][CH2:64][CH2:65][CH2:66][CH2:67][CH2:68][CH2:69][CH2:70][CH2:71][CH2:72][CH3:73])[C:49]([CH3:75])([CH3:74])[CH2:48]2)[N:3]=1.[CH2:76]([CH2:78][NH2:79])[OH:77]>>[OH:77][CH2:76][CH2:78][NH:79][C:2]1[N:7]=[C:6]([NH:8][CH2:9][CH2:10][CH2:11][CH2:12][CH:13]2[CH2:18][C:17]([CH3:19])([CH3:20])[N:16]([O:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH3:39])[C:15]([CH3:40])([CH3:41])[CH2:14]2)[N:5]=[C:4]([NH:42][CH2:43][CH2:44][CH2:45][CH2:46][CH:47]2[CH2:48][C:49]([CH3:74])([CH3:75])[N:50]([O:55][CH2:56][CH2:57][CH2:58][CH2:59][CH2:60][CH2:61][CH2:62][CH2:63][CH2:64][CH2:65][CH2:66][CH2:67][CH2:68][CH2:69][CH2:70][CH2:71][CH2:72][CH3:73])[C:51]([CH3:53])([CH3:54])[CH2:52]2)[N:3]=1

Participants

Reactant 2

HCID 700Ethanolamine

HCID 53812223HCID 53812223, compound

Product 1

HCID 54521421HCID 54521421, compound

Procedure

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

Sources & evidence

ORD record: ord-6eb8a53cc7a94516964586891f93a339
Source dataset: uspto-grants-1994_04
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05300544

Reaction notes

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