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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1465361Generated: November 3, 2026

1-[3-(Trifluoromethyl)phenyl]-4-piperidinone → HCID 57876136, compound

https://huagongshe.com/reaction/1465361

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-[3-(Trifluoromethyl)phenyl]-4-piperidinoneHCID 11053853—
ReactantHCID 68731816HCID 68731816—
SolventEthanolHCID 702—
ProductHCID 57876136HCID 578761368.5%

Reaction Steps

To a stirred solution of N-(4-Chloro-phenyl)-N-[2-(6-methyl-pyridin-3-yl)-ethyl]-hydrazine hydrochloride (0.13 g, 0.5 mmol) in absolute ethanol (5 mL) was added 1-(3-Trifluoromethyl-phenyl)-piperidin-4-one (0.122 g, 0.5 mmol) at RT and then refluxed for 1 h. After completion (TLC), ethanol was evaporated. The crude was purified by preparative HPLC to provide desired compound as brown colored solid (0.02 g, 10% yield) 8-Chloro-5-[2-(6-methyl-pyridin-3-yl)-ethyl]-2-(3-trifluoromethyl-phenyl)-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole (0.020 g, 0.0425 mmol) was dissolved in THF (1.0 mL). A solution of oxalic acid dihydrate (0.0053 g, 0.0425 mmol) in 1.5 mL THF was added and stirred for 30 min at RT. Precipitate was filtered and dried to give oxalate salt as brown solid (0.01 g, 43% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999978B2
Source datasetuspto-grants-2015_04
ORD IDord-acef4f19e8a34203a300a5cda54da924
Source noteuspto-grants-2015_04