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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1276415Generated: October 27, 2026

Potassium Iodide → 1-(3-(10,11-dihyd ro-5 H-dibenz[b,f]azepin-5-yl)-1-propyl)-2-methyl-3-piperidinecarboxylic acid methyl ester

https://huagongshe.com/reaction/1276415

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant5-(3-Chloropropyl)-10,11-dihydro-5H-dibenz[b,f]azepineHCID 286779—
ReactantMethyl 2-methylpiperidine-3-carboxylate hydrochlorideHCID 51358493—
SolventMethyl Ethyl KetoneHCID 6569—
Product1-(3-(10,11-dihyd ro-5 H-dibenz[b,f]azepin-5-yl)-1-propyl)-2-methyl-3-piperidinecarboxylic acid methyl esterHCID 54477109—

Reaction Steps

A mixture of potassium iodide (17.5 g, 0.11 mol) and methyl ethyl ketone (180 ml) was heated at reflux temperature for 1 h. A solution of 5-(3-chloropropyl)-10,11-dihydro-5H-dibenz[b,f]azepine (4.8 g, 0.019 mol, prepared similarly as described in example 1) in methyl ethyl ketone (25 ml) was added and heating at reflux temperature was continued for 2 h. Potassium carbonate (8.5 g, 0.061 mol) and 2-methyl-3-piperidinecarboxylic acid methyl ester hydrochloride (5.1 g, 0.026 mol) were added and the reaction mixture was heated just below reflux temperature for 64 h. After cooling, the reaction mixture was filtered (Hyflo) and the solvent was evaporated in vacuo. The residue was purified by flash chromatography on silica gel (275 g) using a mixture of heptane and ethyl acetate (1:1) as eluent, to give 3.4 g of 1-(3-(10,11-dihydro-5H-dibenz[b,f]-azepin-5-yl)-1-propyl)-2-methyl-3-piperidinecarboxylic acid methyl ester as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06166009
Source datasetuspto-grants-2000_12
ORD IDord-2d47b3fbe51c48b8aa9fb0771d955704
Source noteuspto-grants-2000_12