HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464252Generated: October 29, 2026
Potassium Iodide → HCID 13505772, compound
https://huagongshe.com/reaction/464252
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 1-Phenylpiperazine | HCID 7096 | — |
| Reactant | HCID 13505775 | HCID 13505775 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 13505772 | HCID 13505772 | — |
Reaction Steps
A solution of 2-(4-chlorobutyl)-2,4-dihydro-1H-[1,2,4]triazolo[3,4-c][1,4]benzoxazin-1-one (see example 4, part 1), (1.40 g.; 0.005 mole), potassium iodide (0.83 g.; 0.005 mole) and N-phenylpiperazine (1.79 g.; 0.011 mole) was stirred at 100° C. for 5 hours. The reaction mixture was cooled, poured into water and extracted with methylene chloride. The methylene chloride extracts were combined, washed with dilute brine solution, dried over sodium sulfate and concentrated in vacuo. The resulting residue was chromatographed through 125 g. of silica gel, using a 2% v/v diethylamine in ethyl acetate as eluting liquid. The eluted product thus obtained, titled above, was crystallized in the manner described in example 1, hereinabove, from an ethyl acetate/Skellysolve®B hexane mixture to give 1.56 g., m.p. 89°-90° C. and 0.115 g., m.p. 85°-87° C. of the named, titled compound hereinabove. The analytical sample had melting point 89°-90.5° 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-68f019b803f44c259f9b1139aaacce9a |
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| Source note | uspto-grants-1985_10 |
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