HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzhydrylpiperazine → HCID 67235139, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzhydrylpiperazine | HCID 70048 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | PyBOP | HCID 2724699 | — |
| Reactant | HCID 22646456 | HCID 22646456 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67235139 | HCID 67235139 | — |
Reaction Steps
5-Phenyl-3-(3,4,5-trimethoxybenzoyl)-oxazolidine-4-carboxylic acid (12) (120 mg; 0.310 mmol) is dissolved in methylene chloride (3 mL) at ambient temperature. 1-(Diphenylmethyl)piperazine (94 mg; 0.372 mmol), N,N-diisopropylethylamine (128 mg; 0.99 mmol) and PyBOP (193 mg; 0.372 mmol) are added sequentially. The reaction is stirred for 1 hour at room temperature, then concentrated under reduced pressure. The residue is purified via silica gel chromatography (30%→60% ethyl acetate in hexanes) affording the desired product as a white solid. CIMS: MH+ 622
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06809093B2 |
| Source dataset | uspto-grants-2004_10 |
| ORD ID | ord-e5abc80bf17a4254acba578cb921a85e |
| Source note | uspto-grants-2004_10 |