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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330546Generated: October 31, 2026

Thiophene → HCID 14677571, compound

https://huagongshe.com/reaction/330546

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiopheneHCID 8030—
ReactantNoberastineHCID 60531—
ReactantHCID 178418361HCID 178418361—
ReactantHCID 178486302HCID 178486302—
CatalystPlatinumHCID 23939—
SolventMethanolHCID 887—
ProductHCID 14677571HCID 1467757114.3%

Reaction Steps

A mixture of 2 parts of poly(oxymethylene), 4.5 parts of 3-[(5-methyl-2-furanyl)methyl]-N-(4-piperidinyl)-3H-imidazo[4,5-b]pyridin-2-amine, 1 part of a solution of thiophene in methanol 4% and 120 parts of methanol was hydrogenated at normal pressure and at 50° C. with 2 parts of platinum-on-charcoal catalyst 5%. After the calculated amount of hydrogen was taken up, the catalyst was filtered off over diatomaceous earth and the filtrate was evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol, saturated with ammonia, (96:4 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from acetonitrile, yielding 0.7 parts (14.3%) of 3-[(5-methyl-2-furanyl)methyl]-N-(1-methyl-4-piperidinyl)-3H-imidazo[4,5-b]pyridin-2-amine; mp. 131.0° C. (compound 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04897401
Source datasetuspto-grants-1990_01
ORD IDord-806268a8e1f5495f9798b26239c313a8
Source noteuspto-grants-1990_01