6-Aminohexanoic Acid → HCID 54139582, compound

HRID 1463723Notes

Reaction equation

HRID 1463723 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]([O:30][C:31]2[CH:36]=[CH:35][C:34]([C:37]([C:40]3[CH:45]=[CH:44][C:43]([O:46][C:47]4[N:52]=[C:51](Cl)[N:50]=[C:49]([NH:54][CH2:55][CH2:56][CH2:57][CH2:58][CH:59]5[CH2:64][C:63]([CH3:66])([CH3:65])[N:62]([O:67][CH:68]6[CH2:73][CH2:72][CH2:71][CH2:70][CH2:69]6)[C:61]([CH3:75])([CH3:74])[CH2:60]5)[N:48]=4)=[CH:42][CH:41]=3)([CH3:39])[CH3:38])=[CH:33][CH:32]=2)[N:3]=1.[NH2:76][CH2:77][CH2:78][CH2:79][CH2:80][CH2:81][C:82]([OH:84])=[O:83]>>[C:82]([CH2:81][CH2:80][CH2:79][CH2:78][CH2:77][NH:76][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]([O:30][C:31]2[CH:36]=[CH:35][C:34]([C:37]([C:40]3[CH:45]=[CH:44][C:43]([O:46][C:47]4[N:52]=[C:51]([NH:76][CH2:77][CH2:78][CH2:79][CH2:80][CH2:81][C:82]([OH:84])=[O:83])[N:50]=[C:49]([NH:54][CH2:55][CH2:56][CH2:57][CH2:58][CH:59]5[CH2:64][C:63]([CH3:66])([CH3:65])[N:62]([O:67][CH:68]6[CH2:73][CH2:72][CH2:71][CH2:70][CH2:69]6)[C:61]([CH3:75])([CH3:74])[CH2:60]5)[N:48]=4)=[CH:42][CH:41]=3)([CH3:39])[CH3:38])=[CH:33][CH:32]=2)[N:3]=1)([OH:84])=[O:83]

Participants

3

Reactant 2

HCID 5646-Aminohexanoic AcidHCID 54371226HCID 54371226, compound

Product 1

HCID 54139582HCID 54139582, compound

Procedure

The title compound is prepared from the reaction of 2,2-bis{4-[[2-chloro-4-[N-(1-cyclohexyloxy-2,2,6,6-tetramethylpiperidin-4-yl)butylamino]-1,3,5-triazin-6-yl]oxy]phenyl}propane with 6-aminohexanoic acid.

Sources & evidence

ORD record
ord-3597f903207c4378be9a3a3b20f7121c
Source dataset
uspto-grants-1994_04
Patent number
US05300544

Reaction notes

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