Dimethyl Sulfoxide → HCID 24955418, compound

HRID 2134116Notes

Reaction equation

HRID 2134116 reaction equation
[Br:22][CH2:23][CH2:24][c:25]1[n:26][cH:27][cH:28][cH:29][cH:30]1.[C:31](=[O:32])([O-:33])[O-:34].[CH2:1]([c:2]1[cH:3][cH:4][cH:5][cH:6][cH:7]1)[NH:8][C:9](=[O:10])[c:11]1[c:12]([CH3:21])[n:13][c:14](-[c:16]2[nH:17][n:18][cH:19][cH:20]2)[s:15]1.[CH3:37][S:38](=[O:39])[CH3:40].[CH3:41][CH2:42][O:43][C:44](=[O:45])[CH3:46].[K+:35].[K+:36]>>[CH2:1]([c:2]1[cH:3][cH:4][cH:5][cH:6][cH:7]1)[NH:8][C:9](=[O:10])[c:11]1[c:12]([CH3:21])[n:13][c:14](-[c:16]2[n:17][n:18]([CH2:23][CH2:24][c:25]3[n:26][cH:27][cH:28][cH:29][cH:30]3)[cH:19][cH:20]2)[s:15]1

Participants

7

Reactant 6

HCID 679Dimethyl SulfoxideHCID 813Potassium Cation2×HCID 8857Ethyl AcetateHCID 19660Carbonate IonHCID 129138582-(2-Bromoethyl)pyridineHCID 24955764HCID 24955764, compound

Product 1

HCID 24955418HCID 24955418, compound

Sources & evidence

ORD record
ord-9eb7f98c64574568ba1422b9b257e5e1
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (4/10)

Reaction notes

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