HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464251Generated: October 30, 2026
Potassium Iodide → HCID 13505768, compound
https://huagongshe.com/reaction/464251
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 1,3-Dihydro-1-(4-piperidinyl)-2H-benzimidazol-2-one | HCID 88638 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 13505775 | HCID 13505775 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 13505768 | HCID 13505768 | — |
Reaction Steps
A solution of 2-(4-chlorobutyl)-2,4-dihydro-1H-[1,2,4]triazolo[3,4-c][1,4]benzoxazin-1-one, (1.40 g., 0.005 mole), potassium iodide (0.83 g.; 0.005 mole) and 4-(2-keto-1-benzimidazolinyl)piperidine (2.39 g.; 0.011 mole) in 25 ml. of DMF was warmed to 115° C. and stirred for 4.75 hours. The resulting solution was cooled, poured into saturated sodium bicarbonate aqueous solution and extracted with methylene chloride. The methylene chloride extracts were combined and washed with brine solution, dried over sodium sulfate and concentrated in vacuo. The resulting residue was crystallized from ethyl acetate to give 1.87 g., m.p. 173°-175.5° C. and 0.03 g., m.p. 172°-173° C. of the above named end product. The analytical sample had melting point 174°-175.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04547499 |
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| Source dataset | uspto-grants-1985_10 |
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| ORD ID | ord-aead37b5400348adbe03bf59dd140057 |
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| Source note | uspto-grants-1985_10 |
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