Dimethyl Sulfoxide → HCID 4780303, compound

HRID 136534Notes

Reaction equation

HRID 136534 reaction equation
[Br:1][c:2]1[cH:3][cH:4][c:5]([N+:8](=[O:9])[O-:10])[n:6][cH:7]1.[C:19](=[O:20])([O-:21])[O-:22].[CH2:26]([N+:27]([CH2:28][CH2:29][CH2:30][CH3:31])([CH2:32][CH2:33][CH2:34][CH3:35])[CH2:36][CH2:37][CH2:38][CH3:39])[CH2:40][CH2:41][CH3:42].[CH3:11][CH:12]1[O:13][CH:14]([CH3:18])[CH2:15][NH:16][CH2:17]1.[CH3:43][S:44]([CH3:45])=[O:46].[CH3:47][CH2:48][O:49][C:50](=[O:51])[CH3:52].[I-:25].[K+:23].[K+:24]>>[c:2]1([N:16]2[CH2:15][CH:14]([CH3:18])[O:13][CH:12]([CH3:11])[CH2:17]2)[cH:3][cH:4][c:5]([N+:8](=[O:9])[O-:10])[n:6][cH:7]1

Participants

9

Reactant 8

HCID 679Dimethyl SulfoxideHCID 813Potassium Cation2×HCID 8857Ethyl AcetateHCID 16028TetrabutylammoniumHCID 19660Carbonate IonHCID 30165Iodide IonHCID 1108622,6-DimethylmorpholineHCID 8176205-Bromo-2-nitropyridine

Product 1

HCID 4780303HCID 4780303, compound

Sources & evidence

ORD record
ord-fc0a06c543284293a07f1f81cbb61e22
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (9/10)

Reaction notes

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