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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1772933Generated: October 26, 2026

Ammonia → 2-(2,6-Dimethoxypyridin-4-yl)-2H-pyrido[2,3-e][1,2,4]thiadiazin-3(4H)-one 1,1-dioxide

https://huagongshe.com/reaction/1772933

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant2-Chloropyridine-3-sulfonyl chlorideHCID 10219968—
Reactant2,6-Dimethoxypyridin-4-amineHCID 22220191—
Solvent1,2-DichloroethaneHCID 11—
SolventPyridineHCID 1049—
Product2-(2,6-Dimethoxypyridin-4-yl)-2H-pyrido[2,3-e][1,2,4]thiadiazin-3(4H)-one 1,1-dioxideHCID 9005479120.2%

Reaction Steps

The title compound (2.6 g, 7.73 mmol) was prepared in three steps from 2-chloropyridine-3-sulfonyl chloride (8.24 g, 38.9 mmol) and 2,6-dimethoxypyridin-4-amine (6.0 g, 38.9 mmol) in pyridine (25 mL) at rt; followed by ammonia in an autoclave at 100° C. for 16 h; followed by 1,1′-carbonyldiimidazole (6.2 g, 38.2 mmol) in 1,2-dichloroethane (100 mL) at 90° C. for 16 h using the methods of (IntF1), steps 1 and 2, and (IntA14), step 3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09249160B2
Source datasetuspto-grants-2016_02
ORD IDord-2dcd85fadca244248e3d51d403f277d4
Source noteuspto-grants-2016_02