Ethanolamine → HCID 53819533, compound

HRID 1463694Notes

Reaction equation

HRID 1463694 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]3[CH2:27][CH2:26][CH2:25][CH2:24][CH2:23]3)[C:15]([CH3:29])([CH3:28])[CH2:14]2)[N:5]=[C:4]([NH:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][NH:37][C:38]2[N:43]=[C:42](Cl)[N:41]=[C:40]([NH:45][CH2:46][CH2:47][CH2:48][CH2:49][CH:50]3[CH2:55][C:54]([CH3:57])([CH3:56])[N:53]([O:58][CH:59]4[CH2:64][CH2:63][CH2:62][CH2:61][CH2:60]4)[C:52]([CH3:66])([CH3:65])[CH2:51]3)[N:39]=2)[N:3]=1.[CH2:67]([CH2:69][NH2:70])[OH:68]>>[OH:68][CH2:67][CH2:69][NH:70][C:2]1[N:7]=[C:6]([NH:8][CH2:9][CH2:10][CH2:11][CH2:12][CH:13]2[CH2:14][C:15]([CH3:29])([CH3:28])[N:16]([O:21][CH:22]3[CH2:23][CH2:24][CH2:25][CH2:26][CH2:27]3)[C:17]([CH3:19])([CH3:20])[CH2:18]2)[N:5]=[C:4]([NH:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][NH:37][C:38]2[N:43]=[C:42]([NH:70][CH2:69][CH2:67][OH:68])[N:41]=[C:40]([NH:45][CH2:46][CH2:47][CH2:48][CH2:49][CH:50]3[CH2:55][C:54]([CH3:56])([CH3:57])[N:53]([O:58][CH:59]4[CH2:64][CH2:63][CH2:62][CH2:61][CH2:60]4)[C:52]([CH3:65])([CH3:66])[CH2:51]3)[N:39]=2)[N:3]=1

Participants

3

Reactant 2

HCID 700EthanolamineHCID 54079705HCID 54079705, compound

Product 1

HCID 53819533HCID 53819533, compound

Procedure

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

Sources & evidence

ORD record
ord-16358d7fe1744f67b35a3c4942508d77
Source dataset
uspto-grants-1994_04
Patent number
US05300544

Reaction notes

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