Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Malic Acid | HCID 525 | — |
| Reactant | (Diethylamino)sulfur trifluoride | HCID 123472 | — |
| Reactant | HCID 19006688 | HCID 19006688 | — |
| Reactant | HCID 20087472 | HCID 20087472 | — |
| Reactant | HCID 136169458 | HCID 136169458 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Solvent | Potassium Carbonate | HCID 11430 | — |
| Product | HCID 19006685 | HCID 19006685 | — |
Reaction Steps
A solution of 0.1 mol of 5-heptyloxy-2-(4-(2-hydroxy-5-oxaoctyloxy)-2-fluorophenyl)pyrimidine (prepared by heating optically active 1,2-epoxy-5-oxaoctane, obtainable from malic acid, with 5-heptyloxy-2-(4-hydroxy-2-fluorophenyl)pyrimidine in the presence of dry potassium carbonate and methyl ethyl ketone as solvent) in methylene chloride is cooled to -40° C. and 0.11 mol of DAST is added to it dropwise with moisture being excluded. The reaction mixture is then stirred for 12 hours while heating slowly to room temperature. Then hydrolysis is carried out with ice cooling and the reaction mixture is washed with dilute sodium hydroxide solution and several times with water. After drying over magnesium sulfate, the solvent is removed on a rotary evaporator and the crude product is purified chromatographically and by crystallization. Optically active 5-heptyloxy-2-(4-(2-fluoro-5-oxaoctyloxy)-2-fluorophenyl)pyrimidine is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05340497 |
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| Source dataset | uspto-grants-1994_08 |
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| ORD ID | ord-774950b6f0b44f8fae5b098ca217b904 |
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| Source note | uspto-grants-1994_08 |
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