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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17836Generated: October 26, 2026

Ethylorthoformate → 6,7-dichloro-4-cyclopropyl-4H-1,2,4-benzothiadiazine 1,1-dioxide

https://huagongshe.com/reaction/17836

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylorthoformateHCID 53630039—
Reactant4,5-Dichloro-2-cyclopropylaminobenzenesulphonamideHCID 67529833—
Product6,7-dichloro-4-cyclopropyl-4H-1,2,4-benzothiadiazine 1,1-dioxideHCID 67530650—

Reaction Conditions

Temperature150 °C

Reaction Steps

In a round-bottom flask, a mixture of 4,5-dichloro-2-cyclopropylaminobenzenesulphonamide from the Step above (2.5 g) and ethyl orthoformate (25 mL) is heated in the open state at 150° C. for 1 hour. The suspension obtained is cooled on an ice bath, and the insoluble material is collected by filtration, washed with ether and dried. The solid is re-dissolved in a mixture of acetone and methanol in the hot state and the hot solution is treated with absorbent carbon and then filtered and concentrated to dryness. The residue is recrystallised from methanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741320B2
Source datasetuspto-grants-2010_06
ORD IDord-7b7f45fc90a3465183bb7ac4ccf35df4
Source noteuspto-grants-2010_06