Hydrochloric Acid → N-[5-(2-Amino-4-methyl-1,3-thiazol-5-yl)-2-chloropyridin-3-yl]-5-chloro-1,3-dimethyl-1H-pyrazole-4-sulfonamide

Reaction equation

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

Participants

Reactant 3

HCID 313Hydrochloric Acid

HCID 702Ethanol

HCID 11605316N-{5-[6-chloro-5-(5-chloro-1,3-dimethyl-1H-pyrazol-4-ylsulfonamido)pyridin-3-yl]-4-methyl-1,3-thiazol-2-yl}acetamide

Product 1

HCID 86620391N-[5-(2-Amino-4-methyl-1,3-thiazol-5-yl)-2-chloropyridin-3-yl]-5-chloro-1,3-dimethyl-1H-pyrazole-4-sulfonamide

Sources & evidence

ORD record: ord-b131720d05c848ad86682516305146c1
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (2/10)
DOI: 10.1039/C8SC04228D

Reaction notes

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