Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Propionyl chloride | HCID 62324 | — |
| Reactant | 174458-00-5 | HCID 136381081 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 54041915 | HCID 54041915 | 19.5% |
Reaction Steps
A mixture of 0.33 g of 1-[(tetrahydro-3-furanyl) methyl]-2-(nitroimino)hexahydropyrimidine, 0.07 g of sodium hydride (60%) and 10 ml of acetonitrile was stirred at 50° C. for 30 minutes. After this mixture was cooled on ice, 0.16 g of propionyl chloride was added dropwise thereto over 30 minutes, and the mixture was then stirred at room temperature for 2 hours. After the completion of reaction, insolubles were removed by filtration, and the filtrate was then concentrated under a reduced pressure. The resultant residue was purified by silica gel column chromatography (2:1 ethyl acetate/acetone) to obtain 0.08 g of 1-(ethylcarbonyl)-2-(nitroimino)-3-[(tetrahydro-3-furanyl)methyl]hexahydropyrimidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05614527 |
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| Source dataset | uspto-grants-1997_03 |
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| ORD ID | ord-b071967658df45e48734689561adbf34 |
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| Source note | uspto-grants-1997_03 |
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