HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2187661Generated: November 1, 2026
N-Acetylimidazolidinone → HCID 10308497, compound
https://huagongshe.com/reaction/2187661
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-Acetylimidazolidinone | HCID 79350 | — |
| Reactant | 5-CHLORO-2-(PHENYLMETHYL)-INDOLE | HCID 2762963 | — |
| Solvent | Phosphorus oxychloride | HCID 24813 | — |
| Product | HCID 10308497 | HCID 10308497 | — |
Reaction Steps
A mixture of 2.42 g (10 mmol) 5-chloro-2-benzylindole and 1.28 g (10 mmol) 1-acetyl-imidazolidine-2-one (0.1 mol) is added to phosphorus oxychloride (10 ml) and heated to 60° C. for 5 hours. After evaporation of phosphorus oxychloride the residue is treated with ethanol (14 ml) and heated to reflux for 3.5 hours. Ethanol is evaporated. The residue is purified by chromatography to obtain the hydrochloride. The base is obtainable by treatment with 2N sodium hydroxide to pH 11. The solid is filtered off and dried in vacuo. Hydrochloride, m.p. 299-300° C., M.S. (Ei 70 ev) m/Z M=309.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06410562B1 |
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| Source dataset | uspto-grants-2002_06 |
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| ORD ID | ord-7be9f9623b3349648c940d2d687f8f64 |
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| Source note | uspto-grants-2002_06 |
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