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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26751Generated: October 28, 2026

Thiophene → HCID 23339052, compound

https://huagongshe.com/reaction/26751

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiopheneHCID 8030—
ReactantCyclopentanoneHCID 8452—
ReactantN-(Piperidin-4-yl)pyrimidin-2-amineHCID 18374737—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
ProductHCID 23339052HCID 23339052—

Reaction Steps

To 0.5 parts of a solution of 2 parts of thiophene in 40 parts of ethanol, are added 2 parts of cyclopentanone, 5.5 parts of N-(4-piperidinyl)-2-pyrimidinamine and 120 parts of methanol. The whole is hydrogenated at normal pressure and at room temperature with 2 parts of palladium-on-charcoal 10%. After the calculated amount of hydrogen is taken up, the catalyst is filtered off and the filtrate is evaporated. The residue is taken up in 4-methyl-2-pentanone and a small amount of trichloromethane. The whole is washed twice with a diluted sodium hydroxide solution, dried, filtered and evaporated. The residue is crystallized from 2,2'-oxybispropane. The product is filtered off and dried, yielding 2.3 parts of N-(1-cyclopentyl-4-piperidinyl)-2-pyrimidinamine; mp. 118° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04151286
Source datasetuspto-grants-1979_04
ORD IDord-f8d791ed86564f6688485bff2cc5b045
Source noteuspto-grants-1979_04