HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1160460Generated: October 31, 2026
3,4-dihydro-2H-pyran → HCID 57815104, compound
https://huagongshe.com/reaction/1160460
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3,4-dihydro-2H-pyran | HCID 8080 | — |
| Reactant | Pyridinium.p-toluenesulfonate | HCID 22033616 | — |
| Reactant | HCID 57815131 | HCID 57815131 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57815104 | HCID 57815104 | 69% |
Reaction Steps
The (2R,3S)-2-hydroxy-3-{[3-[methyl(methylsulfonyl)amino]-5-({[(1R)-1-phenylethyl]amino}carbonyl)benzoyl]amino}-4-phenylbutanoic acid methylester obtained in Reference Example 25 2.30 g (4.06 mmol) was dissolved in tetrahydrofuran 8 mL and thereto were added 3,4-dihydro-2H-pyrane 4.80 mL and p-toluenesulfonic acid pyridinium 204 mg (0.81 mmol) and the mixture was stirred under reflux for 8 hours. After distillating tetrahydrofuran off, the residue was extracted by adding ethyl acetate and 5% aqueous sodium carbonate solution. The organic layer was washed with an aqueous saturated sodium chloride solution and dried on magnesium sulfate, filtered and concentrated. The concentrated residue was purified by a column chromatography on silica gel (eluted with chloroform-methanol system) and recrystallized from a mixed solvent of ethyl acetate and hexane. A precipitated material was collected by filtering and dried to give 1.81 g (2.78 mmol) of the title compound (yield: 69%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07816387B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-54dfb36c9f68480480a1beb24298945d |
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| Source note | uspto-grants-2010_10 |
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