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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1793180Generated: November 2, 2026

Phenyl-piperidin-4-yl-methanol → [1-(3-Amino-3-phenyl-propyl)-piperidin-4-yl]-phenyl-methanol

https://huagongshe.com/reaction/1793180

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyl-piperidin-4-yl-methanolHCID 339086—
Reactant478538-78-2HCID 22026034—
Product[1-(3-Amino-3-phenyl-propyl)-piperidin-4-yl]-phenyl-methanolHCID 22026074—

Reaction Steps

The procedure given in Example 2 except for the formation of salts was followed using 3-bromo-1-(tert-butoxycarbonyl)amino-1-phenyl propane and phenyl-piperidin-4-yl-methanol as reactants, instead of d-1-bromo-2-(tert-butoxycarbonyl)amino-3-phenyl propane and hexamethyleneimine to give [1-(3-Amino-3-phenyl-propyl)-piperidin-4-yl]-phenyl-methanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07078537B2
Source datasetuspto-grants-2006_07
ORD IDord-acd83b19b47d45b8a4f04bb5230bd5a2
Source noteuspto-grants-2006_07