Dimethyl Sulfoxide → HCID 66748108, compound

HRID 2152302Notes

Reaction equation

HRID 2152302 reaction equation
[Br:9][CH2:10][CH:11]1[O:12][CH2:13][CH2:14][CH2:15]1.[C:1](=[O:2])([O-:3])[O-:4].[CH3:35][S:36]([CH3:37])=[O:38].[I-:8].[K+:5].[K+:6].[Na+:7].[O:16]=[S:17]1(=[O:34])[N:18]=[C:19]2[N:20]([CH2:21][CH2:22]1)[CH:23]=[CH:24][CH:25]=[C:26]2[c:27]1[cH:28][cH:29][c:30]([OH:33])[cH:31][cH:32]1.[OH2:39]>>[CH2:10]([CH:11]1[O:12][CH2:13][CH2:14][CH2:15]1)[O:33][c:30]1[cH:29][cH:28][c:27]([C:26]2=[CH:25][CH:24]=[CH:23][N:20]3[C:19]2=[N:18][S:17](=[O:16])(=[O:34])[CH2:22][CH2:21]3)[cH:32][cH:31]1

Participants

9

Reactant 8

HCID 679Dimethyl SulfoxideHCID 813Potassium Cation2×HCID 923Sodium ionHCID 962WaterHCID 14501Furan, 2-(bromomethyl)tetrahydro-HCID 19660Carbonate IonHCID 30165Iodide IonHCID 667478174-(2,2-Dioxido-3,4-dihydropyrido[2,1-c][1,2,4]thiadiazin-9-yl)phenol

Product 1

HCID 66748108HCID 66748108, compound

Sources & evidence

ORD record
ord-61d790aad8324c1e8329073410696229
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (4/10)

Reaction notes

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