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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1494656Generated: October 30, 2026

Thiophene → HCID 22368222, compound

https://huagongshe.com/reaction/1494656

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiopheneHCID 8030—
ReactantHCID 14722643HCID 14722643—
ReactantHCID 178418361HCID 178418361—
CatalystPlatinumHCID 23939—
SolventMethanolHCID 887—
ProductHCID 22368222HCID 2236822277.7%

Reaction Steps

A mixture of 7 parts of 3-(aminocarbonyl)-4-[5,5-bis(4-fluorophenyl)pentyl]-N-(2,6-dichloro-4-nitrophenyl)-1-piperazineacetamide, 1 part of a solution of thiophene in methanol 4% and 120 parts of methanol was hydrogenated in a Parr apparatus 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 and the filtrate was evaporated. The residue was converted into the hydrochloride salt in 2-propanol and acetonitrile. The salt was filtered off and dried, yielding 5.55 parts (77.7%) of 3-(aminocarbonyl)-N-(4-amino-2,6-dichlorophenyl)-4-[5,5-bis(4-fluorophenyl)pentyl]-1-piperazineacetamide trihydrochloride; mp. 190.8° C. (compound 84).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05026853
Source datasetuspto-grants-1991_06
ORD IDord-340fdbcc2c4343a18ddc7eb11813e911
Source noteuspto-grants-1991_06