HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330590Generated: October 31, 2026
Iodine → Bis[1-(4-chlorophenyl)-4-(pyrid-3-yl)2,3-diazabutadien-1-yl]disulfide
https://huagongshe.com/reaction/330590
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodine | HCID 807 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 3-[5-(4-Chlorophenyl)-2,3-dihydro-1,3,4-thiadiazol-2-yl]pyridine | HCID 15708363 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Bis[1-(4-chlorophenyl)-4-(pyrid-3-yl)2,3-diazabutadien-1-yl]disulfide | HCID 53981879 | — |
Reaction Steps
3.6 g of powdered potassium hydroxide are added to a solution, cooled to 0° C., of 15 g of the 2-(4-chlorophenyl)-5-(pyrid-3-yl)-4,5-dihydro-1,3,4-thiadiazole prepared according to Example 1a) in 80 ml of acetone. After stirring for ca. 5 minutes at 0°-5° C., 6.9 g of iodine are added in portions and the exothermic reaction is kept at about 0°-5° C. by cooling with ice. The batch is subsequently stirred for 4 hours at ca. 0° C. The precipitated product is isolated by filtration and washed with a small amount of acetone. The crude product is taken up in a 1:3 mixture of tetrahyrofuran/ethyl acetate and the solution is washed once with water and twice with a saturated solution of sodium chloride, dried over sodium sulfate and concentrated by evaporation. The title compound of formula ##STR20## so obtained has a melting point of 143°-145° C. (compound 21).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04897485 |
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| Source dataset | uspto-grants-1990_01 |
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| ORD ID | ord-f972ae0b73d5405a802afb4d13cd9ccc |
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| Source note | uspto-grants-1990_01 |
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