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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 915742Generated: October 25, 2026

1-Bromo-4-fluorobutane → 7-Chloro-4-(4-fluorobutyl)-4H-1,2,4-benzothiadiazine 1,1-dioxide

https://huagongshe.com/reaction/915742

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-4-fluorobutaneHCID 10022—
ReactantPotassium CarbonateHCID 11430—
Reactant7-Chloro-4H-benzo[e][1,2,4]thiadiazine 1,1-dioxideHCID 10036276—
SolventAcetonitrileHCID 6342—
Product7-Chloro-4-(4-fluorobutyl)-4H-1,2,4-benzothiadiazine 1,1-dioxideHCID 69415210—

Reaction Conditions

Temperature100 °C

Reaction Steps

150 mg of the compound obtained in Step A of Example 1 are dissolved in 8 ml of acetonitrile, to which 300 mg of K2CO3 and 0.15 ml of 1-bromo-4-fluorobutane are added. The reaction mixture is introduced into a sealed autoclave and is heated at 100° C. for 3 hours. After cooling, the solvent is evaporated off under reduced pressure and the residue is taken up in a minimum of water. The insoluble material is collected by filtration, washed with water and dried. The precipitate is then recrystallised from a minimum of ethyl acetate with the aid of heat. After cooling, the title compound is collected by filtration, washed with a minimum of ethyl acetate and dried.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07268129B2
Source datasetuspto-grants-2007_09
ORD IDord-d4f40c2eb7f745509f9fcd77489c0491
Source noteuspto-grants-2007_09