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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393985Generated: October 30, 2026

Benzhydrylpiperazine → HCID 131724628, compound

https://huagongshe.com/reaction/393985

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzhydrylpiperazineHCID 70048—
ReactantDiisopropylethylamineHCID 81531—
ReactantPyBOPHCID 2724699—
ReactantHCID 23531924HCID 23531924—
SolventDichloromethaneHCID 6344—
ProductHCID 131724628HCID 131724628—

Reaction Steps

N-(tert-Butoxycarbonyl)-3-phenyl-[(2S)-2-pyrrolidinecarboxylic acid] (14) (1.50 g; 5.1 mmol) prepared according to Chung, J. Y. et al., J. Org Chem. 55:270-5 (1990) is dissolved in methylene chloride (55 mL) at ambient temperature. 1-(Diphenylmethyl)piperazine (1.62 g; 6.4 mmol), N,N-diisopropylethylamine (1.50 g; 2.25 mmol) and PyBOP (3.35 g; 6.4 mmol) are added sequentially. The reaction is stirred for 18 hours at room temperature, then concentrated under reduced pressure. The residue is purified via silica gel chromatography (33%→50% ethyl acetate in hexanes) affording the desired product as a white solid. CIMS: MH+ 526

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06809093B2
Source datasetuspto-grants-2004_10
ORD IDord-1571c08fa5fb4ba490c2273826555b1a
Source noteuspto-grants-2004_10