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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 225754Generated: October 25, 2026

1,3-Benzothiazole-6-sulfonyl chloride → N-(2-Bromo-6-methyl-3-pyridyl)-6-benzothiazolesulfonamide

https://huagongshe.com/reaction/225754

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Benzothiazole-6-sulfonyl chlorideHCID 2795170—
Reactant2-Bromo-6-methylpyridin-3-amineHCID 14418051—
ProductN-(2-Bromo-6-methyl-3-pyridyl)-6-benzothiazolesulfonamideHCID 8662256935%

Reaction Steps

By working in a manner similar to that of Preparation VII, starting with 3-amino-2-bromo-6-methylpyridine and 6-benzothiazolesulfonyl chloride, the expected product is obtained in the form of a beige-colored paste (yield=35%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557122B2
Source datasetuspto-grants-2009_07
ORD IDord-a57f06a4edee43388913997c8df6648f
Source noteuspto-grants-2009_07