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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 893679Generated: October 30, 2026

Thiophene → HCID 13588201, compound

https://huagongshe.com/reaction/893679

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiopheneHCID 8030—
ReactantPotassium AcetateHCID 517044—
ReactantHCID 13588146HCID 13588146—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
ProductHCID 13588201HCID 1358820172.4%

Reaction Steps

A mixture of 1.5 parts of 6-chloro-N4 -[2-[4-[[1[(4-fluorophenyl)methyl]-1H-benzimidazol-2yl]amino]-1piperidinyl]ethyl]4,5-pyrimidinediamine, 3 parts of a solution of thiophene in ethanol 4%, 1 part of potassium acetate and 120 parts of methanol was hydrogenated at normal pressure and at room temperature with 1 part 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 solid residue was taken up in water. The solution was treated with ammonia. The product was extracted with trichloromethane. The organic layer was separated, dried, filtered and evaporated. The residue was crystallized from a mixture of 4-methyl-2-pentanone, yielding 1 part (72.4%) of N4 -[2-[4-[[1[(4fluorophenyl)methyl]-1H-benzimidazol-2-yl]amino]-1-piperidinyl]ethyl]-4,5-pyrimidinediamine; mp. 207.7° C. (intermediate 165).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05126339
Source datasetuspto-grants-1992_06
ORD IDord-636088396b724fcbbc6271b4411716cb
Source noteuspto-grants-1992_06