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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464252Generated: October 29, 2026

Potassium Iodide → HCID 13505772, compound

https://huagongshe.com/reaction/464252

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant1-PhenylpiperazineHCID 7096—
ReactantHCID 13505775HCID 13505775—
SolventWaterHCID 962—
ProductHCID 13505772HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04547499
Source datasetuspto-grants-1985_10
ORD IDord-68f019b803f44c259f9b1139aaacce9a
Source noteuspto-grants-1985_10