HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzhydrylpiperazine → HCID 131724627, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzhydrylpiperazine | HCID 70048 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | PyBOP | HCID 2724699 | — |
| Reactant | HCID 23531923 | HCID 23531923 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 131724627 | HCID 131724627 | — |
Reaction Steps
N-(3,4-Dimethoxybenzenesulfonyl)-[(2S,4S)-4-phenoxy-2-pyrrolidinecarboxylic acid] (10) (0.64 g; 1.57 mmol) is dissolved in methylene chloride (15 mL) at ambient temperature. 1-(Diphenylmethyl)piperazine (0.48 g; 1.89 mmol), N,N-diisopropylethylamine (0.45 g; 3.46 mmol) and PyBOP (0.98 g; 1.89 mmol) are added sequentially. The reaction is stirred for 16 hours at room temperature, then concentrated under reduced pressure. The residue is purified via silica gel chromatography (40%→50% ethyl acetate in hexanes) affording the desired product as a solid foam. CIMS: MH+ 642
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06809093B2 |
| Source dataset | uspto-grants-2004_10 |
| ORD ID | ord-f7614024312b41cd8d1a84945bfcf35b |
| Source note | uspto-grants-2004_10 |