HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 275039Generated: October 26, 2026
Hydrochloric Acid → N-(2,6-Difluorophenyl)-5-formylamino-1,2,4-triazole-3-sulfonamide
https://huagongshe.com/reaction/275039
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2,6-Difluoroaniline | HCID 79647 | — |
| Reactant | HCID 178522608 | HCID 178522608 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | N-(2,6-Difluorophenyl)-5-formylamino-1,2,4-triazole-3-sulfonamide | HCID 178522611 | — |
Reaction Steps
To a mixture of 1.3 g (10 mmol) of 2,6-difluoroaniline in 4 ml of pyridine was added 1.94 g (9.2 mmol) of 5-formylamino-3-chlorosulfonyl-1,2,4-triazole over a period of 5 minutes. The mixture was heated with stirring to 70° C. for 4 hours. It was then cooled and dispersed between 25 ml of 1N aqueous sodium hydroxide and 50 ml of chloroform. The aqueous layer was acidified with aqueous hydrochloric acid and filtered. The solids collected were dried to obtain 167 g (60 percent of theory) of the title compound, m.p. 258°-260° C. The infrared spectrum was consistent with the assigned structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05391759 |
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| Source dataset | uspto-grants-1995_02 |
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| ORD ID | ord-31c4de89595b42dca2ca02089284f578 |
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| Source note | uspto-grants-1995_02 |
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