Hydrogen Bromide → 4-[4-Chloro-3-(2-furylmethylsulfamoyl)-phenyl]-3-methyl-2-methylimino-1,3-thiazolidine-4-ol

Reaction equation

[BrH:1].[CH2:29]([N:30]([CH2:31][CH3:32])[CH2:33][CH3:34])[CH3:35].[Cl:2][c:3]1[c:4]([S:18](=[O:19])(=[O:20])[Cl:21])[cH:5][c:6]([C:9]2([OH:17])[N:10]([CH3:16])[C:11](=[N:14][CH3:15])[S:12][CH2:13]2)[cH:7][cH:8]1.[o:22]1[c:23]([CH2:27][NH2:28])[cH:24][cH:25][cH:26]1>>[Cl:2][c:3]1[c:4]([S:18](=[O:19])(=[O:20])[NH:28][CH2:27][c:23]2[o:22][cH:26][cH:25][cH:24]2)[cH:5][c:6]([C:9]2([OH:17])[N:10]([CH3:16])[C:11](=[N:14][CH3:15])[S:12][CH2:13]2)[cH:7][cH:8]1

Participants

Reactant 4

HCID 260Hydrogen Bromide

HCID 3438Furfurylamine

HCID 8471Triethylamine

HCID 227604902-Chloro-5-(4-hydroxy-3-methyl-2-methylimino-1,3-thiazolidin-4-yl)benzenesulfonyl chloride

Product 1

HCID 227604144-[4-Chloro-3-(2-furylmethylsulfamoyl)-phenyl]-3-methyl-2-methylimino-1,3-thiazolidine-4-ol

Sources & evidence

ORD record: ord-235eb6981c1d4b6899432c7fecaf0ff7
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (8/10)
DOI: 10.1039/C8SC04228D

Reaction notes

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