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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1761437Generated: October 25, 2026

Sodium Iodide → 8-[3-[4-(3-Methylphenyl)-1-piperazinyl]propyloxy]-8-azaspiro[4.5]decan-7,9-dione hydrochloride hemihydrate

https://huagongshe.com/reaction/1761437

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(m-Tolyl)piperazine dihydrochlorideHCID 83110—
Reactant8-(3-Bromopropyloxy)-8-azaspiro[4.5]decan-7,9-dioneHCID 14280583—
CatalystTetrabutylammonium BromideHCID 74236—
SolventAcetonitrileHCID 6342—
SolventTriethylamineHCID 8471—
Product8-[3-[4-(3-Methylphenyl)-1-piperazinyl]propyloxy]-8-azaspiro[4.5]decan-7,9-dione hydrochloride hemihydrateHCID 131715932—

Reaction Steps

A mixture of 8-(3-bromopropyloxy)-8-azaspiro[4.5]decan-7,9-dione (5.0 g), 1-(3-methylphenyl)piperazine dihydrochloride (4.11 g), K2CO3 (9.1 g), NaI (100 mg) and n-Bu4NBr (100 mg) in 100 ml of dry tolune was heated at 80° with stirring under N2. After 4 hours, 50 ml of CH3CN was added. Heating was continued for 18 hr. and 5 ml of Et3N was added. Heating was continued for an additional 6 hr and at which time no starting material remained by TLC. The mixture was cooled to room temperature and filtered. The solvents were removed in vacuo and the residue was chromatographed on silica using ethyl acetate as the eluent. The fractions containing the desired product were combined and concentrated in vacuo.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04826846
Source datasetuspto-grants-1989_05
ORD IDord-1130f591a1a14fe580015499fe06b735
Source noteuspto-grants-1989_05