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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 583075Generated: October 30, 2026

Potassium Carbonate → HCID 44214761, compound

https://huagongshe.com/reaction/583075

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant6-fluoro-3-(1,2,3,6-tetrahydropyridin-4-yl)-1H-indoleHCID 11053072—
ReactantHCID 17777167HCID 17777167—
SolventWaterHCID 962—
ProductHCID 44214761HCID 44214761—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a 25 ml two-necked flask equipped with a reflux condenser and in Argon atmosphere, were added 1-(2-chloroethyl)-3,4-dihydro-7-fluoro-3-(1-methylethyl)-1H-2,1,3-benzothiadiazine-2,2-dioxide(678 mg, 2.2 mmol), 4-(6-fluoroindol-3-yl)-1,2,5,6-tetrahydropyridine (523 mg, 242 mmol), anhydrous K2CO3 (1.09 g, 11 mmol) and 10 ml of deionised water. The mixture was vigorously stirred under Argon for 64 hours at 100° C., allowed to reach room temperature and extracted with EtOAc (3×25 ml). The combined organic extracts were dried (Na2SO4) and solvent removed at reduced pressure. The residue was purified by flash chromatography on silica gel (EtOAc:hexane 1:3) affording 3,4-dihydro-1-{2-[4-(6-fluoroindol-3-yl)-1,2,5,6-tetrahydro-1-pyridyl]-1-ethyl}-3-(1-methylethyl)-7-fluoro-1H-2,1,3-benzothiadiazine-2,2-dioxide as a pale yellow solid, m.p. 103-105°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05929072
Source datasetuspto-grants-1999_07
ORD IDord-20734eaadad643b19d029d97a83b7f6a
Source noteuspto-grants-1999_07