Dimethyl Sulfoxide → HCID 58158548, compound

HRID 1141772Notes

Reaction equation

HRID 1141772 reaction equation
[C:20](=[O:21])([O-:22])[O-:23].[C:36](=[O:37])([O-:38])[OH:39].[CH3:41][S:42](=[O:43])[CH3:44].[Cl:26][c:27]1[cH:28][cH:29][c:30]([N+:33](=[O:34])[O-:35])[n:31][cH:32]1.[Cs+:24].[Cs+:25].[F:1][c:2]1[cH:3][c:4]([NH:9][C:10]([O:11][CH2:12][c:13]2[cH:14][cH:15][cH:16][cH:17][cH:18]2)=[O:19])[cH:5][cH:6][c:7]1[OH:8].[Na+:40].[OH2:45]>>[F:1][c:2]1[cH:3][c:4]([NH:9][C:10]([O:11][CH2:12][c:13]2[cH:14][cH:15][cH:16][cH:17][cH:18]2)=[O:19])[cH:5][cH:6][c:7]1[O:8][c:27]1[cH:28][cH:29][c:30]([N+:33](=[O:34])[O-:35])[n:31][cH:32]1

Participants

9

Reactant 8

HCID 679Dimethyl SulfoxideHCID 769Bicarbonate IonHCID 923Sodium ionHCID 962WaterHCID 19660Carbonate IonHCID 104967Cesium cation2×HCID 2598065-Chloro-2-nitropyridineHCID 58158634HCID 58158634, compound

Product 1

HCID 58158548HCID 58158548, compound

Sources & evidence

ORD record
ord-5ac150214c8e4340aef796207f1aa3f2
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (7/10)

Reaction notes

Loading…