Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium cyanate | HCID 11378442 | — |
| Reactant | HCID 66618552 | HCID 66618552 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 66778849 | HCID 66778849 | — |
Reaction Steps
2.8 g (34.5 mmol, 1.6 eq.) of potassium cyanate are added at 30° C. to a solution of 5 g (21.6 mmol, 1 eq.) of 1-(6-methoxypyridin-3-ylamino)-cyclohexanecarbonitrile in 50 ml of glacial acetic acid. The reaction medium is stirred at 60° C. for 4 hours. 8 ml of hydrochloric acid and then 5 ml of water are added. The medium is heated at 90° C. for 1 hour and then at room temperature for 24 hours. It is then poured into 30 ml of water. The aqueous phase is extracted with ethyl acetate. The organic phases are combined and washed with water. They are dried over sodium sulfate. The solvents are evaporated off. The residue is chromatographed on silica gel (90/10 dichloromethane/methanol). The product is precipitated from dichloromethane and heptane and then filtered off and dried. 1-(6-Methoxypyridin-3-yl)-1,3-diaza-spiro[4.5]decane-2,4-dione is obtained in the form of a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08445523B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-ef18790cef984fdfb52217cb8ad6acff |
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| Source note | uspto-grants-2013_05 |
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