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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 620495Generated: October 29, 2026

Formaldehyde → HCID 13588079, compound

https://huagongshe.com/reaction/620495

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantThiopheneHCID 8030—
ReactantPotassium AcetateHCID 517044—
ReactantHCID 12891714HCID 12891714—
ReactantHCID 178418361HCID 178418361—
CatalystPlatinumHCID 23939—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
ProductHCID 13588079HCID 13588079—

Reaction Steps

To 1 part of a solution of 2 parts of thiophene in 40 parts of ethanol were added 11.3 parts of 1-(4-fluorophenylmethyl)-N-[1-[2-[(phenylmethyl)amino]ethyl]-4-piperidinyl]-1H-benzimidazol-2-amine, 2 parts of paraformaldehyde, 10 parts of potassium acetate and 120 parts of methanol. The whole was hydrogenated at normal pressure and at room temperature with 2 parts of platinum-on-charcoal catalyst 10%. After the calculated amount of hydrogen was taken up, the catalyst was filtered off over Hyflo and the filtrate was evaporated, yielding 9.4 parts of 1-[(4-fluorophenyl)methyl]-N-[1-[2-[methyl(phenylmethyl)amino]ethyl]-4-piperidinyl]-1H-benzimidazol-2-amine as a residue (intermediate 135).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04820822
Source datasetuspto-grants-1989_04
ORD IDord-f0b8fc851bb640838404d1129b68bf62
Source noteuspto-grants-1989_04