Ethanolamine → HCID 54164335, compound

HRID 1463695Notes

Reaction equation

HRID 1463695 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][CH3:29])[C:15]([CH3:31])([CH3:30])[CH2:14]2)[N:5]=[C:4]([NH:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][NH:39][C:40]2[N:45]=[C:44](Cl)[N:43]=[C:42]([NH:47][CH2:48][CH2:49][CH2:50][CH2:51][CH:52]3[CH2:57][C:56]([CH3:59])([CH3:58])[N:55]([O:60][CH2:61][CH2:62][CH2:63][CH2:64][CH2:65][CH2:66][CH2:67][CH3:68])[C:54]([CH3:70])([CH3:69])[CH2:53]3)[N:41]=2)[N:3]=1.[CH2:71]([CH2:73][NH2:74])[OH:72]>>[OH:72][CH2:71][CH2:73][NH:74][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][CH3:29])[C:15]([CH3:31])([CH3:30])[CH2:14]2)[N:5]=[C:4]([NH:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][NH:39][C:40]2[N:45]=[C:44]([NH:74][CH2:73][CH2:71][OH:72])[N:43]=[C:42]([NH:47][CH2:48][CH2:49][CH2:50][CH2:51][CH:52]3[CH2:57][C:56]([CH3:59])([CH3:58])[N:55]([O:60][CH2:61][CH2:62][CH2:63][CH2:64][CH2:65][CH2:66][CH2:67][CH3:68])[C:54]([CH3:70])([CH3:69])[CH2:53]3)[N:41]=2)[N:3]=1

Participants

3

Reactant 2

HCID 700EthanolamineHCID 54188942HCID 54188942, compound

Product 1

HCID 54164335HCID 54164335, compound

Procedure

The title compound is prepared from the reaction of N,N'-bis{2-chloro-4-[N-(1-octyloxy-2,2,6,6-tetramethylpiperidin-4-yl)butylamino]-1,3,5-triazin-6-yl}-1,6-hexanediamine and ethanolamine.

Sources & evidence

ORD record
ord-f6ba3ee9fd374afc9d175bbd61c46396
Source dataset
uspto-grants-1994_04
Patent number
US05300544

Reaction notes

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