Dimethyl Sulfoxide → HCID 68586517, compound

HRID 94232Notes

Reaction equation

HRID 94232 reaction equation
[CH3:36][S:37]([CH3:38])=[O:39].[Cl:18][c:19]1[cH:20][cH:21][c:22]([OH:29])[c:23]([NH:25][C:26](=[O:27])[NH2:28])[cH:24]1.[Cl:1][CH2:2][C:3](=[O:4])[CH:5]1[CH2:6][CH2:7][N:8]([C:11](=[O:12])[O:13][C:14]([CH3:15])([CH3:16])[CH3:17])[CH2:9][CH2:10]1.[K+:30].[K+:31].[O-:32][C:33]([O-:34])=[O:35]>>[CH2:2]([C:3](=[O:4])[CH:5]1[CH2:6][CH2:7][N:8]([C:11](=[O:12])[O:13][C:14]([CH3:15])([CH3:16])[CH3:17])[CH2:9][CH2:10]1)[O:29][c:22]1[cH:21][cH:20][c:19]([Cl:18])[cH:24][c:23]1[NH:25][C:26](=[O:27])[NH2:28]

Participants

6

Reactant 5

HCID 679Dimethyl SulfoxideHCID 813Potassium Cation2×HCID 19660Carbonate IonHCID 11435385(5-Chloro-2-hydroxy-phenyl)-ureaHCID 24229336Tert-butyl 4-(2-chloroacetyl)piperidine-1-carboxylate

Product 1

HCID 68586517HCID 68586517, compound

Sources & evidence

ORD record
ord-d91274ffb9bf4ccbbcfb72e9df41c533
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (2/10)

Reaction notes

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