HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1655068Generated: October 26, 2026
Hydrogen Sulfide → 3-Mercaptopyridine-2-sulfonamide
https://huagongshe.com/reaction/1655068
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Sulfide | HCID 402 | — |
| Reactant | 3-Fluoropyridine-2-sulfonamide | HCID 19957930 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Mercaptopyridine-2-sulfonamide | HCID 127427 | — |
Reaction Steps
1.06 g of hydrogen sulfide are passed at a temperature of +16° to +20° C. under a nitrogen atmosphere into a mixture of 6.88 g of potassium tert-butylate and 5 g of 3-fluoropyridin-2-ylsulfonamide in 90 ml of dimethylformamide. After the mixture has been stirred for 41/2 hours at a temperature of +50° C., 0.32 g of potassium tert-butylate are added and 0.1 g of hydrogen sulfide is passed in. After the reaction mixture has been stirred for 2 hours at a temperature of +50° C., it is concentrated in vacuo at a temperature of +75° C. The resulting oily residue is triturated with 135 ml of cold 0.75N sulfuric acid. After the residue has been filtered and washed with a little water, the resulting product is dried in vacuo over phosphorus pentoxide. This gives 3.58 g of 3-mercaptopyridin-2-ylsulfonamide of a melting point of +102° to +104° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05410063 |
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| Source dataset | uspto-grants-1995_04 |
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| ORD ID | ord-efc3701ebb034da199312f16b9974500 |
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| Source note | uspto-grants-1995_04 |
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