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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256659Generated: October 31, 2026

9-[(4-fluorophenyl)methyl]-8-[[1-(phenylmethyl)-4-piperidinyl]oxy]-9H-purine → 9-[(4-fluorophenyl)methyl]-8-(4-piperidinyloxy)-9H-purine

https://huagongshe.com/reaction/256659

Reaction equation

Participants

RoleNameHCIDCharge
Reactant9-[(4-fluorophenyl)methyl]-8-[[1-(phenylmethyl)-4-piperidinyl]oxy]-9H-purineHCID 19785236—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product9-[(4-fluorophenyl)methyl]-8-(4-piperidinyloxy)-9H-purineHCID 1978523982.2%

Reaction Steps

A mixture of 16.25 parts of 9-[(4-fluorophenyl)methyl]-8-[[1-(phenylmethyl)-4-piperidinyl]oxy]-9H-purine and 200 parts of methanol was hydrogenated at normal pressure and at 50° C. with 3 parts of palladium-on-charcoal catalyst 10% and 6 parts of Raney-nickel catalyst. After the calculated amount of hydrogen was taken up, the catalyst was filtered off and the filtrate was evaporated. The residue was taken up in trichloromethane and water was added. The product was extracted with trichloromethane. The extract was washed with water, dried, filtered and evaporated. The residue was stirred in 1,1'-oxybisethane. The precipitated product was filtered off and dried, yielding 10.5 parts (82.2%) of 9-[(4-fluorophenyl)methyl]-8-(4-piperidinyloxy)-9H-purine; mp. 79.3° C. (compound 56).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05258380
Source datasetuspto-grants-1993_11
ORD IDord-73ca9048d64547b1a7a33f0e22f33de5
Source noteuspto-grants-1993_11