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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17839Generated: October 24, 2026

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

https://huagongshe.com/en/reaction/17839

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylorthoformateHCID 53630039—
Reactant2-Cyclopropylamino-5-nitrobenzenesulphonamideHCID 67530158—
Product4-cyclopropyl-7-nitro-4H-1,2,4-benzothiadiazine 1,1-dioxideHCID 67530771—

Reaction Conditions

Temperature130 °C

Reaction Steps

In a round-bottom flask, a mixture of 2-cyclopropylamino-5-nitrobenzenesulphonamide (5 g), originating from the Step above, and ethyl orthoformate (50 mL) is heated in the open state at 130° C. for 3 hours. The suspension obtained is cooled on an ice bath and the insoluble material is collected by filtration, washed with ether and dried.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741320B2
Source datasetuspto-grants-2010_06
ORD IDord-d3c399511b97447abf51faf290d79fe9
Source noteuspto-grants-2010_06