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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1978542Generated: November 1, 2026

Hydrochloric Acid → N-[1-[3-(4-aminophenyl)propan-1-yl]piperidin-4-yl]-5-thia-1,8b-diazaacenaphthylene-4-carboxamide trihydrochloride

https://huagongshe.com/reaction/1978542

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantN-[1-[3-(4-tert-butoxycarbonylaminophenyl)propan-1-yl]piperidin-4-yl]-5-thia-1,8b-diazaacenaphthylene-4-carboxamideHCID 21994165—
SolventEthanolHCID 702—
ProductN-[1-[3-(4-aminophenyl)propan-1-yl]piperidin-4-yl]-5-thia-1,8b-diazaacenaphthylene-4-carboxamide trihydrochlorideHCID 2199390571%

Reaction Steps

Concentrated hydrochloric acid (1.5 ml) was added to N-[1-[3-(4-tert-butoxycarbonylaminophenyl)propan-1-yl]piperidin-4-yl]-5-thia-1,8b-diazaacenaphthylene-4-carboxamide (350 mg, 0.656 mmol) and the mixture was stirred at room temperature for 2 hours. Ethanol was added to the mixture to give N-[1-[3-(4-aminophenyl)propan-1-yl]piperidin-4-yl]-5-thia-1,8b-diazaacenaphthylene-4-carboxamide trihydrochloride as orange crystals (251 mg, 71%), which were collected by filtration and washed with ethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06235731B1
Source datasetuspto-grants-2001_05
ORD IDord-19e87ca0cd0a4dc0b6b408fa70a1b3b0
Source noteuspto-grants-2001_05