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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2262707Generated: November 2, 2026

Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate → 2-[1-(4-Acetyl-phenyl)-piperidin-4-yl]-1-(4-cyclobutyl-piperazin-1-yl)-ethanone

https://huagongshe.com/reaction/2262707

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
Reactant1-CyclopentylpiperazineHCID 806421—
Reactant[1-(4-Acetyl-phenyl)-piperidin-4-YL]-acetic acidHCID 49759600—
SolventDichloromethaneHCID 6344—
Product2-[1-(4-Acetyl-phenyl)-piperidin-4-yl]-1-(4-cyclobutyl-piperazin-1-yl)-ethanoneHCID 57442404—

Reaction Steps

To a solution of [1-(4-acetyl-phenyl)-piperidin-4-yl]-acetic acid (0.11 mmol) in anhydrous DCM (2 mL) is added 1-cyclopentylpiperazine (1.1 eq.), TEA (0.22 mmol), and BOP (0.14 mmol). The resulting mixture is stirred at rt overnight. DCM is evaporated. The residue is dissolved in EtOAc (20 mL), washed with water (5 mL×3) and brine, dried over sodium sulfate, and concentrated. The crude product is purified through PTLC to give the title compound. 1H NMR (300 MHz, CDCl3) δ 7.85 (2H, d), 6.85 (2H, d), 3.89 (2H, br), 3.66 (2H, t), 3.49 (2H, t), 2.91 (2H, dt), 2.46˜2.57 (8H, overlapped), 2.26 (2H, d), 2.12 (1H, m), 1.22˜1.95 (12H, m); LC-MS (M+1) 398.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07851474B2
Source datasetuspto-grants-2010_12
ORD IDord-560002b7921b493fa74d17edcb3fa32d
Source noteuspto-grants-2010_12