HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1818771Generated: November 2, 2026
Sulfamide → 1-(2-Fluorophenyl)-1,3-dihydro-2,1,3-benzothiadiazole 2,2-dioxide
https://huagongshe.com/reaction/1818771
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfamide | HCID 82267 | — |
| Reactant | N1-(2-Fluorophenyl)benzene-1,2-diamine | HCID 19039441 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Diglyme | HCID 8150 | — |
| Product | 1-(2-Fluorophenyl)-1,3-dihydro-2,1,3-benzothiadiazole 2,2-dioxide | HCID 46833094 | 23.3% |
Reaction Steps
Dry diglyme (10 mL) was added to a flask equipped with a dropping funnel under a nitrogen atmosphere and brought to a vigorous reflux N-(2-fluorophenyl)benzene-1,2-diamine (1.2 g, 6.0 mmol) and sulfamide (0.69 g, 7.2 mmol) were dissolved in 5 mL of diglyme and placed in the dropping funnel. The mixture was added dropwise to the flask over 15 minutes and then refluxing was continued for an additional 15 minutes. The mixture was cooled to ambient temperature and diluted with ether, washed with water, 2N HCl, water, brine, dried over anhydrous magnesium sulfate, and concentrated. The crude product was purified via Isco chromatography (Redisep, silica, gradient 5-50% (ethyl acetate containing 2% formic acid) in hexane) to afford 1-(2-fluorophenyl)-1,3-dihydro-2,1,3-benzothiadiazole 2,2-dioxide (0.37 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07601722B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-74c91b520f1d4741a148da04c0ec3175 |
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| Source note | uspto-grants-2009_10 |
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