HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl bromoacetate → HCID 67458407, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Potassium bis(trimethylsilyl)amide | HCID 3251421 | — |
| Reactant | HCID 67463033 | HCID 67463033 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67458407 | HCID 67458407 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
4-{(S)-2-[(6-cyclopentyloxy-2-phenyl-pyrimidine-4-carbonyl)-amino]-4-hydroxy-butyryl}-piperazine-1-carboxylic acid ethyl ester (16.8 mg) was dissolved in THF (1 ml) under argon and cooled to 0° C. A solution of potassium bis-(trimethylsilyl)-amide (0.5 M in toluene, 8 μl) and, 5 min later, ethylbromoacetate (5 μl) were added. The mixture was stirred at 0° C. for 1 h and evaporated off. The residue was taken up in water and extracted twice with EA. The org. layers were washed with water, a NaCl solution, dried (Na2SO4) and evaporated off to give 19 mg of the desired compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08048881B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-69a294d6c746478c8c7bcaf3d5ed4263 |
| Source note | uspto-grants-2011_11 |