HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → (S,S)-2-(3-allyl-2-oxo-piperazin-1-yl)-3-naphthalen-2-yl-propionic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Mercaptophenol | HCID 240147 | — |
| Reactant | (S,S)-2-[3-Allyl-4-(2-nitro-benzenesulfonyl)-2-oxo-piperazin-1-yl]-3-naphthalen-2-yl-propionic acid methyl ester | HCID 25133905 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (S,S)-2-(3-allyl-2-oxo-piperazin-1-yl)-3-naphthalen-2-yl-propionic acid methyl ester | HCID 25131150 | 79% |
Reaction Steps
To a solution of (S,S)-2-[3-allyl-4-(2-nitro-benzenesulfonyl)-2-oxo-piperazin-1-yl]-3-naphthalen-2-yl-propionic acid methyl ester, 4, (4.8 g, 8.9 mmol) and 4-mercaptophenol (4.5 g, 35.7 mmol) in DMF (35 mL) is added potassium carbonate (7.4 g, 53.4 mmol). The reaction mixture is stirred 18 hours then quenched with saturated NaHCO3 solution and extracted with EtOAc (200 mL). The extract is dried over Na2SO4 and concentrated in vacuo to afford a bright yellow oil which is purified over silica gel (hexanes/EtOAc, 1:1 to EtOAc/MeOH, 10:1) to afford 2.45 g (79% yield) of the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07132539B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-d7bb79702a3f4033a9fe245fa21d0623 |
| Source note | uspto-grants-2006_11 |