HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 68928242, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | tert-Butyl bromoacetate | HCID 79177 | — |
| Reactant | HCID 68930909 | HCID 68930909 | — |
| Reactant | (2S)-1-(Diphenylmethyl)-2-methylpiperazine | HCID 68933826 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 68928242 | HCID 68928242 | — |
| Product | HCID 68933233 | HCID 68933233 | — |
Reaction Steps
To a solution of a mixture of (S)-1-benzhydryl-2-methylpiperazine and (S)-1-benzhydryl-3-methylpiperazine (490 mg, 1.839 mmol) in 25 mL of MeCN was added tert-butyl bromoacetate (356 μl, 2.207 mmol), followed by slow addition of triethylamine (384 μl, 2759 μmol). The reaction mixture was stirred at rt overnight. The solution was evaporated to dryness and the residual was submitted to flash chromatography (SiO2, DCM to DCM/EtOAc=100:3 to 100:5 to 100:10) to give (S)-tert-butyl 2-(4-benzhydryl-3-methylpiperazin-1-yl)acetate as a colorless oil and (S)-tert-butyl 2-(4-benzhydryl-2-methylpiperazin-1-yl)acetate as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07538114B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-3b448b2efeac4c57a67f36a3cf66f3bd |
| Source note | uspto-grants-2009_05 |