HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 4-benzyloxycarbonyl-3-(S)-methoxymethyl-1-[(2-methylthiopyrimidin-5-yl)-methyl]-piperazine-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 60209911 | HCID 60209911 | — |
| Reactant | 4-Benzyloxycarbonyl-3-(S)-methoxymethyl-piperazine-2-one | HCID 68898261 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-benzyloxycarbonyl-3-(S)-methoxymethyl-1-[(2-methylthiopyrimidin-5-yl)-methyl]-piperazine-2-one | HCID 68900376 | 33% |
Reaction Steps
4-Benzyloxycarbonyl-3-(S)-methoxymethyl-piperazine-2-one (0.1 g 0.37 mmol), 5-bromomethyl-2-methylthiopyrimidine (0.08 g, 0.37 mmol) and tetra-n-butylammonium bromide (0.06 g, 0.19 mmol) are placed in dichloromethane (1 mL) and 50% aqueous NaOH (0.03 mL) and stirred for 4 h. The mixture is diluted with water and is extracted with dichloromethane (2×20 mL). The combined organic extracts are dried (MgSO4) and are evaporated. The residue is purified by flash chromatography (silica gel, 98:2 dichloromethane/methanol) to provide the intermediate title compound as a colorless oil (0.05 g, 33%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07612075B2 |
| Source dataset | uspto-grants-2009_11 |
| ORD ID | ord-a172bc08fb7d400e8ae0e97920553fde |
| Source note | uspto-grants-2009_11 |