Dimethyl Sulfoxide → HCID 18617544, compound

HRID 687754Notes

Reaction equation

HRID 687754 reaction equation
[C:10](#[N:11])[c:12]1[cH:13][nH:14][c:15]2[cH:16][cH:17][c:18]([CH2:21][CH2:22][NH:23][C:24]([c:25]3[cH:26][cH:27][c:28](-[c:31]4[n:32][c:33]([Cl:37])[n:34][cH:35][cH:36]4)[cH:29][cH:30]3)=[O:38])[cH:19][c:20]12.[CH3:39][S:40]([CH3:41])=[O:42].[O:1]=[C:2]1[N:3]([CH2:7][CH2:8][NH2:9])[CH2:4][CH2:5][NH:6]1>>[O:1]=[C:2]1[N:3]([CH2:7][CH2:8][NH:9][c:33]2[n:32][c:31](-[c:28]3[cH:27][cH:26][c:25]([C:24]([NH:23][CH2:22][CH2:21][c:18]4[cH:17][cH:16][c:15]5[nH:14][cH:13][c:12]([C:10]#[N:11])[c:20]5[cH:19]4)=[O:38])[cH:30][cH:29]3)[cH:36][cH:35][n:34]2)[CH2:4][CH2:5][NH:6]1

Participants

4

Reactant 3

HCID 679Dimethyl SulfoxideHCID 80480N-(2-Aminoethyl)ethyleneureaHCID 18617562N-[2-(3-Cyano-1H-indol-5-yl)-ethyl]-4-[2-chloropyrimidin-4-yl]benzamide

Product 1

HCID 18617544HCID 18617544, compound

Sources & evidence

ORD record
ord-57b14185f70145eea42c9d989b28c58c
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (3/10)

Reaction notes

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