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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1153873Generated: October 25, 2026

Isopropylamine → Indecainide

https://huagongshe.com/reaction/1153873

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropylamineHCID 6363—
Reactant6'-hydroxyspiro(9H-fluorene-9,3'-piperidine)-2'-oneHCID 13368041—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
ProductIndecainideHCID 52195—

Reaction Steps

The general procedure described above was followed when 6'-Hydroxyspiro-(9H-fluorene-9,3'-piperidine)-2'-one (2.7 g) was dissolved in isopropylamine (350 ml) and 10% palladium on charcoal (0.3 g) was added and the vessel pressurized to 90 p.s.i. with hydrogen. The reaction mixture was then heated at 40° for 16 hours and then allowed to cool to room temperature. The catalyst was removed by filtration and the isopropylamine evaporated under reduced pressure. The resulting residue was dissolved in dichloromethane (20 ml) washed with water (2×50 ml), dried with anhydrous sodium sulphate and evaporated to dryness under reduced pressure. The residue was triturated with hexane to give 9-carbamoyl-9-(3-isopropylaminopropyl)fluorene crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04486592
Source datasetuspto-grants-1984_12
ORD IDord-47769892be5f43c789762af7af4517e3
Source noteuspto-grants-1984_12