Dimethyl Sulfoxide → HCID 22353315, compound

HRID 201875Notes

Reaction equation

HRID 201875 reaction equation
[C:1]([CH3:2])(=[O:3])[NH:4][CH2:5][CH2:6][NH:7][c:8]1[cH:9][c:10]([NH:20][C:21]([C:22]([O:24][CH3:23])=[O:25])=[O:26])[n:11][c:12](-[c:14]2[cH:15][cH:16][cH:17][cH:18][cH:19]2)[n:13]1.[CH3:42][S:43]([CH3:44])=[O:45].[Cl:39][CH2:40][Cl:41].[c:27]1([N:33]2[CH2:34][CH2:35][NH:36][CH2:37][CH2:38]2)[cH:28][cH:29][cH:30][cH:31][cH:32]1>>[C:1]([CH3:2])(=[O:3])[NH:4][CH2:5][CH2:6][NH:7][c:8]1[cH:9][c:10]([NH:20][C:21]([C:22](=[O:24])[N:36]2[CH2:35][CH2:34][N:33]([c:27]3[cH:28][cH:29][cH:30][cH:31][cH:32]3)[CH2:38][CH2:37]2)=[O:26])[n:11][c:12](-[c:14]2[cH:15][cH:16][cH:17][cH:18][cH:19]2)[n:13]1

Participants

5

Reactant 4

HCID 679Dimethyl SulfoxideHCID 6344DichloromethaneHCID 70961-PhenylpiperazineHCID 20811457HCID 20811457, compound

Product 1

HCID 22353315HCID 22353315, compound

Sources & evidence

ORD record
ord-660e131d68aa42fb8220cddbf2898c46
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (6/10)

Reaction notes

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