Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Bis(2-oxo-3-oxazolidinyl)phosphinic chloride | HCID 152842 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 178419562 | HCID 178419562 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178464137 | HCID 178464137 | 72% |
Reaction Steps
To a solution of the compound of Example 8 (200 mg, 0.32 mmol) in dichloromethane (5 mL) and N,N-dimethylformamide (5 mL) were added excess amount of dimethylamine and bis-(2-oxo-3-oxazolidinyl)-phosphinic chloride (325.2 mg, 1.27 mmol), and the mixture was stirred at room temperature for 28 hours. To the reaction solution was added saturated aqueous sodium bicarbonate, and the mixture was extracted with ethyl acetate-toluene (1:1). The organic layer was dried over anhydrous magnesium sulfate, and then filtered and concentrated, and the resulting residue was purified by silica gel column chromatography (chloroform/methanol/ammonia water=20/1/0 to 10/1/0 to 200/10/1 to 100/10/1). To the purified substance were added tetrahydrofuran and 1M hydrochloric acid (1 mL), and the mixture was concentrated. The resulting solid was suspended in diethyl ether, and then filtered to give the titled compound (139.0 mg, 72%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07825155B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-40a32d686c334b3c98c8d9b43b1c679d |
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| Source note | uspto-grants-2010_11 |
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