HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2398536Generated: October 30, 2026
Potassium Hydroxide → HCID 21433254, compound
https://huagongshe.com/reaction/2398536
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-Methylthio-2-imidazoline hydroiodide | HCID 88369 | — |
| Reactant | 2-(2,4-dioxo-3,1-benzoxazin-1-yl)ethyl acetate | HCID 12226000 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 21433254 | HCID 21433254 | — |
Reaction Steps
A mixture of 18 g. of N-(2-acetoxyethyl)isatoic anhydride, 8.5 g. of 2-methylmercapto-imidazoline and 2 pellets of potassium hydroxide in 300 ml. of dioxane is heated at reflux for 5 hours, the solvent then evaporated off and water added. The resulting precipitate is recovered by filtering and washed twice with water. The precipitate is dissolved in methylene chloride and extracted 3times with 1N. hydrochloric solution. The combined hydrochloric acid solutions and filtered through celite, sodium carbonate solution is added and the resulting precipitate is recovered by filtering, washed with water, air dried, dissolved in methylene chloride, dried, filtered and the methylene chloride exchanged for diethyl ether. The resulting precipitate is recovered by filtering, washed with cold diethyl ether and dried under reduced pressure at 40° C. to obtain 10-(2'-acetoxyethyl)-2,3-dihydro-imidazo[2,1-b] quinazolin-5(10H)-one, m.p. 124°-126° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04025511 |
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| Source dataset | uspto-grants-1977_05 |
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| ORD ID | ord-a8ee9f31ec244117b5d532a2a1e49cca |
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| Source note | uspto-grants-1977_05 |
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