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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17840Generated: October 27, 2026

4-cyclopropyl-7-nitro-4H-1,2,4-benzothiadiazine 1,1-dioxide → 7-amino-4-cyclopropyl-4H-1,2,4-benzothiadiazine 1,1-dioxide

https://huagongshe.com/reaction/17840

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-cyclopropyl-7-nitro-4H-1,2,4-benzothiadiazine 1,1-dioxideHCID 67530771—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product7-amino-4-cyclopropyl-4H-1,2,4-benzothiadiazine 1,1-dioxideHCID 67528972—

Reaction Steps

To a solution of 4-cyclopropyl-7-nitro-4H-1,2,4-benzothiadiazine 1,1-dioxide (5 g; prepared in Step C of Example 41) in ethanol (180 mL) there is added 10 % palladium-on-carbon (500 mg). The suspension is placed in a hydrogenator under 10 atmospheres of H2 for 30 minutes at ambient temperature. The suspension is concentrated to dryness under reduced pressure and the residue is taken up in boiling acetone (300 mL). The insoluble material is removed by filtration in the hot state and is washed with boiling acetone. The filtrate is concentrated to dryness and the residue is recrystallised from methanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741320B2
Source datasetuspto-grants-2010_06
ORD IDord-31614994462e491a9d22cce00641e013
Source noteuspto-grants-2010_06