Acetate → N-(5-bromo-2-chloro-3-pyridinyl)methanesulfonamide

HRID 2328916Notes

Reaction equation

HRID 2328916 reaction equation
[Br:1][c:2]1[cH:3][c:4]([NH2:9])[c:5]([Cl:8])[n:6][cH:7]1.[C:21](=[O:22])([O-:23])[O-:24].[CH2:34]1[O:35][CH2:36][CH2:37][O:38][CH2:39]1.[CH3:16][S:17]([Cl:18])(=[O:19])=[O:20].[CH3:29][C:30](=[O:31])[O-:32].[CH3:40][OH:41].[ClH:27].[K+:25].[K+:26].[Na+:28].[OH2:33].[cH:10]1[cH:11][cH:12][n:13][cH:14][cH:15]1>>[Br:1][c:2]1[cH:3][c:4]([NH:9][S:17]([CH3:16])(=[O:19])=[O:20])[c:5]([Cl:8])[n:6][cH:7]1

Participants

12

Reactant 11

HCID 175AcetateHCID 313Hydrochloric AcidHCID 813Potassium Cation2×HCID 887MethanolHCID 923Sodium ionHCID 962WaterHCID 1049PyridineHCID 19660Carbonate IonHCID 312751,4-DioxaneHCID 31297Methanesulfonyl chlorideHCID 218583543-Amino-5-bromo-2-chloropyridine

Product 1

HCID 59519513N-(5-bromo-2-chloro-3-pyridinyl)methanesulfonamide

Sources & evidence

ORD record
ord-bd34ecb40ce34a2a80bbf530ea1cd502
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (10/10)

Reaction notes

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