Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1655895Generated: October 31, 2026

Ethyl 2-(4-cyanomethyl-3,4-dihydro-3-oxo-2H-1,4-benzothiazin-2-yl)acetate → Ethyl 2-[4-(5,7-difluorobenzothiazol-2-yl)methyl-3,4-dihydro-3-oxo-2H-1,4-benzothiazin-2-yl]acetate

https://huagongshe.com/reaction/1655895

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-(4-cyanomethyl-3,4-dihydro-3-oxo-2H-1,4-benzothiazin-2-yl)acetateHCID 10062806—
Reactant2-Amino-4,6-difluorothiophenol hydrochlorideHCID 19789641—
SolventEthanolHCID 702—
ProductEthyl 2-[4-(5,7-difluorobenzothiazol-2-yl)methyl-3,4-dihydro-3-oxo-2H-1,4-benzothiazin-2-yl]acetateHCID 1002591876%

Reaction Steps

Ethyl 2-(4-cyanomethyl-3,4-dihydro-3-oxo-2H-1,4-benzothiazin-2-yl)acetate (580 mg) and 474 mg of 2-amino-4,6-difluorothiophenol hydrochloride were added to 4 ml of anhydrous ethanol, the mixture was heated to reflux under argon atmosphere. After 15 hours, the solvent was distilled off. Water was added to the mixture, and extracted with ethyl acetate. After the drying of the organic layer over anhydrous magnesium sulfate, the solvent was distilled off. The resulting oily matter was subjected to alumina column chromatography. Elution with hexane-ehtyl acetate gave 660 mg of the title compound. The structural formula and physical data of this compound are shown in Table 19.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05252571
Source datasetuspto-grants-1993_10
ORD IDord-a295049dbe98494986e41762927628fc
Source noteuspto-grants-1993_10