Ethanolamine → (2-Hydroxyethyl)amino-4,6-bis{N-[1-(alpha-methylbenzyloxy)-2,2,6,6-tetramethylpiperidin-4-yl]butylamino}-1,3,5-triazine

HRID 1587235Notes

Reaction equation

HRID 1587235 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][CH:22]([CH3:29])[C:23]3[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=3)[C:15]([CH3:31])([CH3:30])[CH2:14]2)[N:5]=[C:4]([NH:32][CH2:33][CH2:34][CH2:35][CH2:36][CH:37]2[CH2:42][C:41]([CH3:44])([CH3:43])[N:40]([O:45][CH:46]([CH3:53])[C:47]3[CH:52]=[CH:51][CH:50]=[CH:49][CH:48]=3)[C:39]([CH3:55])([CH3:54])[CH2:38]2)[N:3]=1.[CH2:56]([CH2:58][NH2:59])[OH:57]>>[OH:57][CH2:56][CH2:58][NH:59][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][CH:22]([CH3:29])[C:23]3[CH:24]=[CH:25][CH:26]=[CH:27][CH:28]=3)[C:15]([CH3:30])([CH3:31])[CH2:14]2)[N:5]=[C:4]([NH:32][CH2:33][CH2:34][CH2:35][CH2:36][CH:37]2[CH2:38][C:39]([CH3:54])([CH3:55])[N:40]([O:45][CH:46]([CH3:53])[C:47]3[CH:52]=[CH:51][CH:50]=[CH:49][CH:48]=3)[C:41]([CH3:43])([CH3:44])[CH2:42]2)[N:3]=1

Participants

3

Reactant 2

HCID 700EthanolamineHCID 539761142-chloro-4,6-bis{N-[1-(alpha-methylbenzyloxy)-2,2,6,6-tetramethylpiperidin-4-yl]butylamino}-1,3,5-triazine

Product 1

HCID 54085206(2-Hydroxyethyl)amino-4,6-bis{N-[1-(alpha-methylbenzyloxy)-2,2,6,6-tetramethylpiperidin-4-yl]butylamino}-1,3,5-triazine

Procedure

The title compound is prepared from the reaction of 2-chloro-4,6-bis{N-[1-(α-methylbenzyloxy)-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-7c53e468501f4c5aa1925acb6d5ad3a2
Source dataset
uspto-grants-1993_06
Patent number
US05216156

Reaction notes

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