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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2248820Generated: October 26, 2026

Thiophene → HCID 178480440, compound

https://huagongshe.com/reaction/2248820

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiopheneHCID 8030—
ReactantPotassium AcetateHCID 517044—
ReactantHCID 178418361HCID 178418361—
ReactantHCID 178419280HCID 178419280—
ReactantHCID 178486302HCID 178486302—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 178480440HCID 17848044056%

Reaction Steps

A mixture of 3 parts of poly(oxymethylene), 5 parts of 7-[(4-fluorophenyl)methyl]-8-(4-piperidinylamino)-7H-purin-6-ol dihydrobromide, 1 part of a solution of thiophene in methanol 4%, 5 parts of potassium acetate and 120 parts of methanol was hydrogenated at normal pressure and at room temperature with 2 parts of palladium-on-charcoal catalyst 10%. 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 water and the whole was treated with sodium carbonate. The product was extracted with dichloromethane. The extract was dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol, saturated with ammonia, (95:5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from acetonitrile. The product was filtered off and dried, yielding 2 parts (56%) of 7-[(4-fluorophenyl)methyl]-8-[(1-methyl-4-piperidinyl)amino] -7H-purin-6-ol; mp. 255.6° C. (compound 139).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05041448
Source datasetuspto-grants-1991_08
ORD IDord-123e5bee36d1496f84f5d9e814e18fd8
Source noteuspto-grants-1991_08