Ethanolamine → HCID 19090186, compound

HRID 1463699Notes

Reaction equation

[CH3:1][O:2][N:3]1[C:8]([CH3:10])([CH3:9])[CH2:7][CH:6]([N:11]([C:55]2[N:60]=[C:59](Cl)[N:58]=[C:57]([NH:62][CH2:63][CH2:64][CH2:65][CH2:66][CH:67]3[CH2:72][C:71]([CH3:74])([CH3:73])[N:70]([O:75][CH3:76])[C:69]([CH3:78])([CH3:77])[CH2:68]3)[N:56]=2)[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][N:18]([CH:43]2[CH2:48][C:47]([CH3:50])([CH3:49])[N:46]([O:51][CH3:52])[C:45]([CH3:54])([CH3:53])[CH2:44]2)[C:19]2[N:24]=[C:23](Cl)[N:22]=[C:21]([NH:26][CH2:27][CH2:28][CH2:29][CH2:30][CH:31]3[CH2:36][C:35]([CH3:38])([CH3:37])[N:34]([O:39][CH3:40])[C:33]([CH3:42])([CH3:41])[CH2:32]3)[N:20]=2)[CH2:5][C:4]1([CH3:80])[CH3:79].[CH2:81]([CH2:83][NH2:84])[OH:82]>>[CH3:1][O:2][N:3]1[C:8]([CH3:10])([CH3:9])[CH2:7][CH:6]([N:11]([C:55]2[N:60]=[C:59]([NH:84][CH2:83][CH2:81][OH:82])[N:58]=[C:57]([NH:62][CH2:63][CH2:64][CH2:65][CH2:66][CH:67]3[CH2:72][C:71]([CH3:74])([CH3:73])[N:70]([O:75][CH3:76])[C:69]([CH3:78])([CH3:77])[CH2:68]3)[N:56]=2)[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][N:18]([CH:43]2[CH2:48][C:47]([CH3:50])([CH3:49])[N:46]([O:51][CH3:52])[C:45]([CH3:54])([CH3:53])[CH2:44]2)[C:19]2[N:24]=[C:23]([NH:84][CH2:83][CH2:81][OH:82])[N:22]=[C:21]([NH:26][CH2:27][CH2:28][CH2:29][CH2:30][CH:31]3[CH2:36][C:35]([CH3:38])([CH3:37])[N:34]([O:39][CH3:40])[C:33]([CH3:42])([CH3:41])[CH2:32]3)[N:20]=2)[CH2:5][C:4]1([CH3:80])[CH3:79]

Participants

Reactant 2

HCID 700Ethanolamine

HCID 53723043HCID 53723043, compound

Product 1

HCID 19090186HCID 19090186, compound

Procedure

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

Sources & evidence

ORD record: ord-ad4379e2c6fc4ada869b4e68ec782988
Source dataset: uspto-grants-1994_04
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05300544

Reaction notes

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