Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydantoin | HCID 10006 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2-Chloro-N-(1,2,3,4-tetrahydroacridin-9-yl)acetamide | HCID 14471301 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 15116191 | HCID 15116191 | 73.8% |
Reaction Steps
In 20 ml of dimethylformamide was suspended 0.8 g (content: 60%) of sodium hydride, and then 3 g of 2,4-imidazolidinedione was added to the suspension and the mixture was stirred at room temperature for 30 minutes. Then, 2.75 g of 9-chloroacetylamino-1,2,3,4-tetrahydroacridine (described in "Chem. listy, Vol. 51, p. 1906 (1957)") was added to the mixture and reaction was carried out by heating to 80° C. for 30 minutes. After cooling to 10° C., the mixture was poured into 100 ml of an aqueous solution containing 8 g of ammonium chloride. Precipitated crystals were collected by filtration, washed with water and dried. These crystals were recrystallized from methanol-chloroform to give 2.5 g of the title compound. Melting point: 302° to 304° C. (decomposed).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04985430 |
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| Source dataset | uspto-grants-1991_01 |
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| ORD ID | ord-e66c2877938f4f2096c6d2f8de351bc2 |
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| Source note | uspto-grants-1991_01 |
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