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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2209975Generated: October 31, 2026

Tetrahydrofuran → 6-amino-4-[2-[4-(1H-indol-3-yl)-1-piperidinyl]ethyl]-2(1H)-quinolinone

https://huagongshe.com/reaction/2209975

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant4-[2-[4-(1H-indol-3-yl)-1-piperidinyl]ethyl]-6-nitro-2(1H)-quinolinoneHCID 19379678—
SolventMethanolHCID 887—
Product6-amino-4-[2-[4-(1H-indol-3-yl)-1-piperidinyl]ethyl]-2(1H)-quinolinoneHCID 1937969377.3%

Reaction Conditions

Temperature55 °C

Reaction Steps

Into a mixed solvent of tetrahydrofuran (800 ml) and methanol (200 ml) was dissolved 4-[2-[4-(1H-indol-3-yl)-1-piperidinyl]ethyl]-6-nitro-2(1H)-quinolinone (III-19) (6 g, 14.4 mmol) under heating. Paladium on carbon (2.5 g) was added thereto and the mixture was stirred under hydrogen atmosphere at 55 ° C. for 4 hours. The reaction mixture was filtered at the same temperature and the solvent was distilled off from the filtrate. The residue was dried and then recrystallized from a mixture of methanol, THF and water to give the desired product (III-20) (4.3 g) as pale yellow crystals (mp 214°-216 ° C. (methanol/tetrahydrofuran water)). Yield 77.3 %.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05457099
Source datasetuspto-grants-1995_10
ORD IDord-ac9aff5d334c4a528ded1df787b81043
Source noteuspto-grants-1995_10