3-(4-Acetyl-piperazin-1-yl)-propionic acid → HCID 66760558, compound

HRID 1122809Notes

Reaction equation

HRID 1122809 reaction equation
[C:35]([CH3:36])(=[O:37])[N:38]1[CH2:39][CH2:40][N:41]([CH2:44][CH2:45][C:46](=[O:47])[OH:48])[CH2:42][CH2:43]1.[Cl:49][c:50]1[c:51]([CH2:52][O:53][c:54]2[c:55]3[n:56][c:57]([O:58][CH3:59])[n:60]([CH2:61][c:62]4[cH:63][cH:64][cH:65][cH:66][n:67]4)[c:68]3[cH:69][cH:70][cH:71]2)[c:72]([Cl:73])[cH:74][cH:75][c:76]1[N:77]([CH3:78])[C:79](=[O:80])[CH2:81][NH:82][C:83](=[O:84])[CH2:85][CH2:86][c:87]1[cH:88][cH:89][c:90]([C:91]([NH:92][CH2:93][CH2:94][O:95][CH3:96])=[O:97])[cH:98][cH:99]1.[NH2:1][CH2:2][C:3](=[O:4])[N:5]([CH3:6])[c:7]1[c:8]([Cl:34])[c:9]([CH2:14][O:15][c:16]2[cH:17][cH:18][cH:19][c:20]3[n:21]([CH2:27][c:28]4[n:29][cH:30][cH:31][cH:32][cH:33]4)[c:22]([O:25][CH3:26])[n:23][c:24]23)[c:10]([Cl:13])[cH:11][cH:12]1>>[NH:1]([CH2:2][C:3](=[O:4])[N:5]([CH3:6])[c:7]1[c:8]([Cl:34])[c:9]([CH2:14][O:15][c:16]2[cH:17][cH:18][cH:19][c:20]3[n:21]([CH2:27][c:28]4[n:29][cH:30][cH:31][cH:32][cH:33]4)[c:22]([O:25][CH3:26])[n:23][c:24]23)[c:10]([Cl:13])[cH:11][cH:12]1)[C:46]([CH2:45][CH2:44][N:41]1[CH2:40][CH2:39][N:38]([C:35]([CH3:36])=[O:37])[CH2:43][CH2:42]1)=[O:47]

Participants

4

Reactant 3

HCID 20506993-(4-Acetyl-piperazin-1-yl)-propionic acidHCID 667603852-amino-N-(2,4-dichloro-3-(((2-methoxy-1-(pyridin-2-ylmethyl)-1H-benzo[d]imidazol-4-yl)oxy)methyl)phenyl)-N-methylacetamideHCID 667609784-(3-((2-((2,4-dichloro-3-(((2-methoxy-1-(pyridin-2-ylmethyl)-1H-benzo[d]imidazol-4-yl)oxy)methyl)phenyl)(methyl)amino)-2-oxoethyl)amino)-3-oxopropyl)-N-(2-methoxyethyl)benzamide

Product 1

HCID 66760558HCID 66760558, compound

Sources & evidence

ORD record
ord-2571086738aa4eb2b29ccaa0d0d8e1ba
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (7/10)

Reaction notes

Loading…