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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2233272Generated: October 31, 2026

Thiophene → HCID 18452754, compound

https://huagongshe.com/reaction/2233272

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiopheneHCID 8030—
ReactantHCID 2885971HCID 2885971—
CatalystPalladiumHCID 23938—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18452754HCID 1845275487%

Reaction Steps

A mixture of 1-(2-naphthalenylsulfonyl)-4-(4-nitrophenyl)-piperazine (7.5 mmol) in THF (150 ml) was hydrogenated at 50° C. with Pd/C 10% (1 g) as a catalyst in the presence of thiophene solution (0.5 ml). After uptake of H2 (3 equiv.), the catalyst was filtered off and the filtrate was evaporated. The residue was crystallized from 2-propanol. The formed precipitate was filtered off, washed with 2-propanol and dried (55° C., vacuum), yielding 2.39 g (87%) of 1-(4-aminophenyl)-4-(2-naphthalenylsulfonyl)-piperazine (interm. 7).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07709487B2
Source datasetuspto-grants-2010_05
ORD IDord-0d7fb85947d6403986b099f76cda1899
Source noteuspto-grants-2010_05