Dimethyl Sulfoxide → HCID 17968178, compound

HRID 1240089Notes

Reaction equation

HRID 1240089 reaction equation
[Br:21][CH2:22][c:23]1[cH:24][c:25]2[c:26]([n:27][c:28]([C:31]#[N:32])[n:29][cH:30]2)[n:33]1[CH2:34][C:35]([CH3:36])([CH3:37])[CH3:38].[C:15](=[O:16])([O-:17])[O-:18].[CH2:1]([CH3:2])[N:3]1[C:4](=[O:14])[NH:5][C:6](=[O:13])[C:7]12[CH2:8][CH2:9][NH:10][CH2:11][CH2:12]2.[CH3:39][S:40]([CH3:41])=[O:42].[K+:19].[K+:20]>>[CH2:1]([CH3:2])[N:3]1[C:4](=[O:14])[NH:5][C:6](=[O:13])[C:7]12[CH2:8][CH2:9][N:10]([CH2:22][c:23]1[cH:24][c:25]3[c:26]([n:27][c:28]([C:31]#[N:32])[n:29][cH:30]3)[n:33]1[CH2:34][C:35]([CH3:36])([CH3:37])[CH3:38])[CH2:11][CH2:12]2

Participants

6

Reactant 5

HCID 679Dimethyl SulfoxideHCID 813Potassium Cation2×HCID 19660Carbonate IonHCID 113128256-Bromomethyl-7-(2,2-dimethyl-propyl)-7H-pyrrolo[2,3-d]pyrimidine-2-carbonitrileHCID 17968236HCID 17968236, compound

Product 1

HCID 17968178HCID 17968178, compound

Sources & evidence

ORD record
ord-86c458bf17834db38e8a5b40de9fe5b3
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (5/10)

Reaction notes

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