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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Bromo-4-fluorobutane | HCID 10022 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 7-Chloro-4H-benzo[e][1,2,4]thiadiazine 1,1-dioxide | HCID 10036276 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 7-Chloro-4-(4-fluorobutyl)-4H-1,2,4-benzothiadiazine 1,1-dioxide | HCID 69415210 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07268129B2 |
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| Source dataset | uspto-grants-2007_09 |
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| ORD ID | ord-d4f40c2eb7f745509f9fcd77489c0491 |
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| Source note | uspto-grants-2007_09 |
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