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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 367178Generated: October 28, 2026

Thionyl Chloride → 2-(1,2,3,4-tetrahydroquinolin-1-yl)-4H-pyrido[3,2-e]-1,3-thiazin-4-one monohydrate

https://huagongshe.com/reaction/367178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant2-Chloronicotinic acidHCID 76258—
Reactant6,8-Dibromo-1,2,3,4-tetrahydroquinolineHCID 23287644—
ReactantHCID 178514171HCID 178514171—
SolventAcetoneHCID 180—
SolventDimethylformamideHCID 6228—
Product2-(1,2,3,4-tetrahydroquinolin-1-yl)-4H-pyrido[3,2-e]-1,3-thiazin-4-one monohydrateHCID 2328763884.3%

Reaction Steps

The reaction procedure of Example 57 was followed except that 1.339 g (8.5 mmol) of 2-chloronicotinic acid, 13 ml of thionyl chloride, two droplets of DMF, 680 mg of ammonium isothiocyanate, 13 ml of acetone, 2.473 g of 6,8-dibromo-1,2,3,4-tetrahydroquinoline and 8 ml of acetone were used. The product was then recrystallized from a mixture of ethanol and hexane to obtain 2.244 g of 2-(1,2,3,4-tetrahydroquinolin-1-yl)-4H-pyrido[3,2-e]-1,3-thiazin-4-one monohydrate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06133258
Source datasetuspto-grants-2000_10
ORD IDord-8c653e1fff9c4f9fa8e057e880f88459
Source noteuspto-grants-2000_10