Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 13670001 | HCID 13670001 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 13670002 | HCID 13670002 | 72.9% |
Reaction Steps
Added at room temperature to a suspension of 0.80 (21 mmol) of lithium aluminum hydride in THF (20 ml) was 1.5 g of 5,6-dihydro-6-ethyl-5-oxo-2-(4-benzylpiperazino)pyrido[4,3-d]pyrimidine (Referential Example 11). After refluxing the reaction mixture for 4 hours, the reaction mixture was added with water to decompose excess lithium aluminum hydride. An aqueous solution of sodium hydroxide and chloroform were added to the resultant mixture to extract the latter. After washing the chloroform layer with water, it was dried with anhydrous magnesium sulfate and was then concentrated to obtain 1.4 g of light yellowish crystals. The crude crystals were immersed in ethyl acetate to obtain 1.1 g of 1,4,5,6-Tetrahydro-6-ethyl-5-oxo-2-(4-benzylpiperazino)pyrido[4,3-d]pyrimidine as colorless crystals (yield: 72%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04734418 |
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| Source dataset | uspto-grants-1988_03 |
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| ORD ID | ord-ec7fc31f5a574931be41b1535021f65f |
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| Source note | uspto-grants-1988_03 |
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