Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 68723Generated: November 1, 2026

6-(4-(1-benzhydrylazetidin-3-yl)piperazin-1-yl)-3-ethyl-1-phenyl-1H-pyrazolo[3,4-d]pyrimidine → HCID 58483585, compound

https://huagongshe.com/reaction/68723

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-(4-(1-benzhydrylazetidin-3-yl)piperazin-1-yl)-3-ethyl-1-phenyl-1H-pyrazolo[3,4-d]pyrimidineHCID 67447954—
CatalystPalladium ChlorideHCID 24290—
CatalystPalladium hydroxideHCID 9942167—
SolventAcetic AcidHCID 176—
ProductHCID 58483585HCID 58483585—

Reaction Steps

A 100-mL round-bottom flask was purged, flushed and maintained with a hydrogen atmosphere, then, was added a solution of 6-(4-(1-benzhydrylazetidin-3-yl)piperazin-1-yl)-3-ethyl-1-phenyl-1H-pyrazolo[3,4-d]pyrimidine (400 mg, 0.76 mmol, 1.00 equiv) in acetic acid (20 mL) at room temperature. To the resulting mixture was then added Pd(OH)2 (50 mg, 0.4 mmol, 0.5 equiv), in portions at room temperature, followed by PdCl2 (50 mg, 0.28 mmol, 0.37 equiv), in portions at room temperature. The resulting solution was stirred overnight at room temperature. The solids were filtered out. The resulting mixture was concentrated under vacuum. The resulting residue (250 mg) was purified by Prep-HPLC with the following conditions (Gilson Pre-HPLC): Column, SHISEIDO, CAPCELL PAK C18, 20 mm ID*250 mm, 5 u; mobile phase, methanol/H2O; Detector, UV 254 nm, to yield 6-(4-(azetidin-3-yl)piperazin-1-yl)-3-ethyl-1-phenyl-1H-pyrazolo[3,4-d]pyrimidine as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822447B2
Source datasetuspto-grants-2014_09
ORD IDord-290367fa991c4689a09b4f39cececd9d
Source noteuspto-grants-2014_09