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HRID 363312作成日:2026年10月26日

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/363312

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium IodideHCID 4875—
反応物Potassium CarbonateHCID 11430—
反応物5-(3-Chloropropyl)-10,11-dihydro-5H-dibenz[b,f]azepineHCID 286779—
反応物Methyl 2-methylpiperidine-3-carboxylate hydrochlorideHCID 51358493—
溶媒Methyl Ethyl KetoneHCID 6569—
生成物1-(3-(10,11-dihyd ro-5 H-dibenz[b,f]azepin-5-yl)-1-propyl)-2-methyl-3-piperidinecarboxylic acid methyl esterHCID 54477109—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05874428
出典データセットuspto-grants-1999_02
ORD IDord-4a3adc4d803e43d386a0a4b565f109ab
出典メモuspto-grants-1999_02