Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Pyrithione | HCID 1570 | — |
| Edukt | Oxalyl chloride | HCID 65578 | — |
| Edukt | Sodium | HCID 5360545 | — |
| Katalysator | Dimethylformamide | HCID 6228 | — |
| Katalysator | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Lösungsmittel | Benzene | HCID 241 | — |
| Produkt | 2,2'-Thiodipyridine | HCID 521114 | 72% |
Reaktionsschritte
360 mg (1 mmol) of peracetoquinic acid (32) are taken into solution with stirring in 5 ml of benzene with the addition of 1 ml of oxalyl chloride and 1 drop of DMF for 3 hours. After evaporation to dryness, the residue is taken up in 5 ml of benzene and added with stirring to a suspension of 180 mg (1.1 mmol) of the sodium salt of N-hydroxypyridine-2-thione and 12 mg (0.1 mmol) of DMAP. The reaction mixture is kept refluxing in 10 ml of toluuene under an atmosphere of nitrogen. After 2 hours of heating under reflux, the cooled reaction mixture is filtered on Celite and evaporated to dryness. By flash chromatography on silica (90% of CH2Cl2 ; 10% EtOAc), 306 mg of pyridyl sulfide of formula (34) are obtained in the form of a yellowish oil. Yield 72%.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04668356 |
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| Quelldatensatz | uspto-grants-1987_05 |
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| ORD ID | ord-f97cda4dac004f19a4353661f6288300 |
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| Quellennotiz | uspto-grants-1987_05 |
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