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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1075875Generated: October 31, 2026

Sodium Iodide → 1-{2-[4-(10,11-Dihydro-3-methoxy-8-methylthio-dibenzo[b,f]thiepin-10-yl)-1-piperazinyl]-ethyl}-2-pyrrolidinone

https://huagongshe.com/reaction/1075875

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(2-Chloroethyl)pyrrolidin-2-oneHCID 3156650—
Reactant1-(10,11-Dihydro-3-methoxy-8-methylthio-dibenzo[b,f]thiepin-10-yl)-piperazineHCID 13498245—
SolventTolueneHCID 1140—
Product1-{2-[4-(10,11-Dihydro-3-methoxy-8-methylthio-dibenzo[b,f]thiepin-10-yl)-1-piperazinyl]-ethyl}-2-pyrrolidinoneHCID 21416201—

Reaction Steps

11 G. of 1-(10,11-dihydro-3-methoxy-8-methylthio-dibenzo[b,f]thiepin-10-yl)-piperazine are heated together with 15 g. of potassium carbonate, 0.5 g. of sodium iodide, 11 g. of N-(β-chloroethyl)-2-pyrrolidinone and 100 ml. of toluene under reflux conditions for 17 hours. Then, the mixture is evaporated under reduced pressure. The residue is partitioned between water and ether, and the ethereal phase dried over sodium sulfate and evaporated. The residue obtained is chromatographed with chloroform over aluminum oxide. The 1-{2-[4-(10,11-dihydro-3-methoxy-8-methylthio-dibenzo[b,f]thiepin-10-yl)-1-piperazinyl]-ethyl}-2-pyrrolidinone thus obtained is converted into the corresponding dihydrochloride by reaction with hydrogen chloride. The resulting dihydrochloride melts at 202°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03954764
Source datasetuspto-grants-1976_05
ORD IDord-4ce7f1fc5d7647a9aac5fd9517c262b8
Source noteuspto-grants-1976_05