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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066169Generated: October 26, 2026

2-Aminopyridine → 7-Chloro-3-(pyrid-2-yl)amino-4H-1,2,4-benzothiadiazine 1,1-dioxide

https://huagongshe.com/reaction/1066169

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminopyridineHCID 10439—
Reactant7-Chloro-3-methylsulfinyl-4H-1,2,4-benzothiadiazine 1,1-dioxideHCID 21197903—
Solvent3-ChlorotolueneHCID 7931—
Product7-Chloro-3-(pyrid-2-yl)amino-4H-1,2,4-benzothiadiazine 1,1-dioxideHCID 11109629—

Reaction Steps

7-Chloro-3-methylsulfinyl-4H-1,2,4-benzothiadiazine 1,1-dioxide (0.25 g) and 2-aminopyridine (0.25 g) in 3-chlorotoluene (5 mL) was heated at 150° C. for 1 h. After cooling, the white precipitate was collected by filtration and washed with diethylether. The insoluble material was dissolved in 1M NaOH (20 mL), treated with charcoal, filtered, and the filtrate was adjusted to pH 3 with 6N HCl. The precipitate was collected by filtration, washed with water, dissolved in hot DMF (15 mL), mixed with an equal volume of distilled water and cooled. The white precipitate was collected by filtration, washed with water and dried (yield: 0.12 g); m.p. >310° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06242443B1
Source datasetuspto-grants-2001_06
ORD IDord-92da720591f6476c88608fb152406d38
Source noteuspto-grants-2001_06