HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 614845Generated: October 30, 2026
2-Pyridinamine, 5-iodo- → HCID 28412369, compound
https://huagongshe.com/reaction/614845
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Pyridinamine, 5-iodo- | HCID 88579 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 178418616 | HCID 178418616 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 28412369 | HCID 28412369 | — |
Reaction Steps
11.0 G. (0.05 moles) of 2-amino-5-iodo pyridine, 6.1 g. (0.055 moles) of 2-mercapto pyridine, 2.97 g. (0.055 moles) of sodium methoxide and 1.0 g. of copper powder are combined in 200 ml. of methanol and heated at 150° C. for 12 hours in a glass lined bomb. The reaction mixture is filtered and the filtrate evaporated to dryness in vacuo. The residue is dissolved in 300 ml. of methylenechloride and washed 5 times with 2.5 N sodium hydroxide and 3 times with saturated sodium chloride solution. The methylene chloride is dried over magnesium sulfate, and evaporated to dryness. The residue is dissolved in boiling methanol, treated with decolorizing carbon, filtered and evaporated to dryness affording 2-amino-5-(2-pyridylthio) pyridine, m.p. 121° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04146642 |
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| Source dataset | uspto-grants-1979_03 |
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| ORD ID | ord-7728afb6d73d44f6a97421fe6a6d8faf |
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| Source note | uspto-grants-1979_03 |
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