Dimethyl Sulfoxide → HCID 68457795, compound

HRID 176891Notes

Reaction equation

HRID 176891 reaction equation
[C:1]([CH3:2])([CH3:3])([CH3:4])[O:5][C:6](=[O:7])[N:8]1[CH2:9][CH2:10][CH:11]([NH:14][C:15]([c:16]2[cH:17][c:18]([O:24][CH2:25][C:26]#[N:27])[cH:19][c:20]([O:22][CH3:23])[cH:21]2)=[O:28])[CH2:12][CH2:13]1.[C:29]([O-:30])(=[O:31])[O-:32].[CH3:37][S:38]([CH3:39])=[O:40].[K+:33].[K+:34].[OH:35][OH:36]>>[C:1]([CH3:2])([CH3:3])([CH3:4])[O:5][C:6](=[O:7])[N:8]1[CH2:9][CH2:10][CH:11]([NH:14][C:15]([c:16]2[cH:17][c:18]([O:24][CH2:25][C:26]([NH2:27])=[O:30])[cH:19][c:20]([O:22][CH3:23])[cH:21]2)=[O:28])[CH2:12][CH2:13]1

Participants

6

Reactant 5

HCID 679Dimethyl SulfoxideHCID 784Hydrogen PeroxideHCID 813Potassium Cation2×HCID 19660Carbonate IonHCID 684560424-(3-Cyanomethoxy-5-methoxy-benzoylamino)-piperidine-1-carboxylic acid tert-butyl ester

Product 1

HCID 68457795HCID 68457795, compound

Sources & evidence

ORD record
ord-1a31ce9223bd4e9283c75bbeaf623a02
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (6/10)

Reaction notes

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