Hydrogen Bromide → 2-Bromo-5-chloro-6-n-propylsulfamoyl-1-indanone

Reaction equation

[Br:20].[BrH:1].[CH3:21][CH2:22][O:23][C:24](=[O:25])[CH3:26].[Cl:2][c:3]1[cH:4][c:5]2[c:9]([cH:10][c:11]1[S:12]([NH:13][CH2:14][CH2:15][CH3:16])(=[O:17])=[O:18])[C:8](=[O:19])[CH2:7][CH2:6]2>>[Br:1][CH:7]1[CH2:6][c:5]2[cH:4][c:3]([Cl:2])[c:11]([S:12]([NH:13][CH2:14][CH2:15][CH3:16])(=[O:17])=[O:18])[cH:10][c:9]2[C:8]1=[O:19]

Participants

Reactant 3

HCID 260Hydrogen Bromide2×

HCID 8857Ethyl Acetate

HCID 227563895-Chloro-6-n-propylsulfamoyl-1-indanone

Product 1

HCID 227563962-Bromo-5-chloro-6-n-propylsulfamoyl-1-indanone

Sources & evidence

ORD record: ord-b3061d0c056e4a4cb1cd937e54038a3d
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (9/10)
DOI: 10.1039/C8SC04228D

Reaction notes

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