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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256648Generated: October 30, 2026

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

https://huagongshe.com/reaction/256648

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantDimethylacetamideHCID 31374—
Reactant1-Benzylpiperidin-4-olHCID 78461—
Reactant9-[(4-fluorophenyl)methyl]-8-(methylthio)-9H-purineHCID 19785232—
SolventWaterHCID 962—
Product9-[(4-fluorophenyl)methyl]-8-[[1-(phenylmethyl)-4-piperidinyl]oxy]-9H-purineHCID 1978523661.1%

Reaction Steps

A mixture of 12.6 parts of 1-(phenylmethyl)-4-piperidinol, 3.2 parts of a sodium hydride dispersion 50% and 200 parts of N,N-dimethylacetamide was stirred for 1 hour at room temperature. 18 Parts of 9-[(4-fluorophenyl)methyl]-8-(methYlthio)-9H-purine were added portionwise and upon completion, stirring was continued for 4 hours at room temperature. The reaction mixture was poured into water. The product was filtered off and taken up in trichloromethane. The organic layer was washed with water and filtered over diatomaceous earth. The filtrate was dried, filtered and evaporated. After crystallization from acetonitrile, the product was filtered off and dried, yielding 16.75 parts (61.1%) of 9-[(4-fluorophenyl)methyl]-8-[[1-(phenylmethyl)-4-piperidinyl]oxy]-9H-purine; mp. 117.0° C. (compound 5).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05258380
Source datasetuspto-grants-1993_11
ORD IDord-619cbb9fa50c4f2d9e3ef47a0deb49d2
Source noteuspto-grants-1993_11