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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1767655Generated: October 31, 2026

Hydrochloric Acid → HCID 178464506, compound

https://huagongshe.com/reaction/1767655

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 178464508HCID 178464508—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 178464506HCID 17846450695%

Reaction Steps

3-Cyclohexyl-7-(N,N-diethylsulphamoyl)-5-formyl-1,2-dihydro-1,2,4-benzothiadiazine-1,1-dioxide (0.20 g, 0.46 mmol) was dissolved in 99% EtOH (60 ml). One small drop of concentrated hydrochloric acid was added to ensure fully hydrogenation. The mixture was hydrogenated using Pd/C (10%, 10 mg) at 4 bar pressure for 24 h. The mixture was filtered through a pad of Celite T and evaporated to dryness. The residue was dissolved in EtOAc (50 ml) and washed with water (10 ml), dried (Na2SO4) and evaporated to dryness yielding 0.18 mg (95%) of 3-cyclohexyl-7-(N,N-diethylsulphamoyl)-5-methyl-1,2-dihydro-1,2,4-benzothiadiazine-1,1-dioxide as colorless powder. The product was further transformed by Method F. M.p. 206–208° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07235548B2
Source datasetuspto-grants-2007_06
ORD IDord-bae1b1fda1204e8dbbcd02ce8d92092a
Source noteuspto-grants-2007_06