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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2248807Generated: October 30, 2026

Hydrogen Bromide → HCID 178420878, compound

https://huagongshe.com/reaction/2248807

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantHCID 19785281HCID 19785281—
SolventAcetic AcidHCID 176—
ProductHCID 178420878HCID 178420878—

Reaction Steps

A mixture of 24.8 parts of 4-[[9-[(4-fluorophenyl)methyl]-9H-purin-8-yl]thio]-1-[(4-methylphenyl)sulfonyl]piperidine and 300 parts of acetic acid, saturated with hydrogen bromide was stirred overnight at room temperature. After evaporation, the residue was taken up in water. The whole was treated with a sodium hydroxide solution and extracted with dichloromethane. The extract was acidified with a hydrochloric acid solution and extracted with water. The aqueous layer was treated with a sodium hydroxide solution and the product was extracted with dichloromethane. The extract was washed with water, dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol, (95:5 by volume)→trichloromethane and methanol, saturated with ammonia, (90:10 by volume) as eluents. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from acetonitrile. The product was filtered off and dried, yielding 3.0 parts (17.4%) of 9-[(4-fluorophenyl)methyl[-8-(4-piperidinylthio)-9H-purine; mp. 113.5° C. (compound 31).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05041448
Source datasetuspto-grants-1991_08
ORD IDord-8b04de644a9245adb47d790c1ed872cd
Source noteuspto-grants-1991_08