HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Piperidone → 2-(3-Methoxypropoxy)-N-{3-methyl-2(S)-[2-oxo-5(S)-(2-oxopiperidin-1-ylmethyl)-oxazolidin-4(S)-ylmethyl]butyl}benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Piperidone | HCID 12665 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | tert-butyl (3(S)-{[2-(3-methoxypropoxy)benzoylamino]methyl}-4-methyl-1(S)-(R)-oxiranylpentyl)-carbamate | HCID 86613450 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 2-(3-Methoxypropoxy)-N-{3-methyl-2(S)-[2-oxo-5(S)-(2-oxopiperidin-1-ylmethyl)-oxazolidin-4(S)-ylmethyl]butyl}benzamide | HCID 68623980 | — |
Reaction Steps
A mixture of 0.115 g of piperidin-2-one, 0.136 g of potassium tert-butoxide in 3 ml of dimethyl sulphoxide is stirred at room temperature over 30 minutes, admixed with 0.26 g of tert-butyl (3(S)-{[2-(3-methoxypropoxy)benzoylamino]methyl}-4-methyl-1(S)—(R)-oxiranylpentyl)-carbamate (Example 1b) and subsequently stirred further at room temperature overnight. The reaction mixture is poured onto ice-water and extracted with tert-butyl methyl ether (2×). The combined organic phases are washed successively with water and brine, dried over sodium sulphate and concentrated by evaporation. The title compound is identified from the residue by means of flash chromatography (SiO2 60F) on the basis of the Rf value.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07786307B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-787a7e4668c44104b35774cb236b783b |
| Source note | uspto-grants-2010_08 |