Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Isobutyryl chloride | HCID 62325 | — |
| Reactant | 174458-00-5 | HCID 136381081 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 54151898 | HCID 54151898 | 45.2% |
Reaction Steps
A mixture of 2.2 g of 1-[(tetrahydro-3-furanyl) methyl]-2-(nitroimino)hexahydropyrimidine, 0.58 g of sodium hydride (60%) and 100 ml of acetonitrile was stirred at 50° C. for 30 minutes. After this mixture was cooled on ice, 1.58 g of isobutanoyl 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 concentration was then carried out under a reduced pressure. The resultant residue was purified by silica gel column chromatography (2:1 ethyl acetate/acetone) to obtain 1.30 g of 1-(isopropylcarbonyl)-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-6a2cf560a30643a8ba2699055411f21c |
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| Source note | uspto-grants-1997_03 |
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