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HRID 736790作成日:2026年10月26日

Sodium Iodide → methyl 1-(10,11-dihydro5H-dibenzo[a,d][7]annulen-5-yl)-1,2,5,6-tetrahydropyridine-3-carboxylate

https://huagongshe.com/reaction/736790

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium IodideHCID 5238—
反応物TriethylamineHCID 8471—
反応物5H-Dibenzo(a,d)cycloheptene, 10,11-dihydro-5-chloro-HCID 14587—
反応物Norarecoline HydrochlorideHCID 201540—
溶媒1,4-DioxaneHCID 31275—
生成物methyl 1-(10,11-dihydro5H-dibenzo[a,d][7]annulen-5-yl)-1,2,5,6-tetrahydropyridine-3-carboxylateHCID 6881668255%

反応条件

温度90 °C

反応手順

A mixture of methyl 1,2,5,6-tetrahydropyridine-3-carboxylate hydrochloride (crude, 150 mmol), 5-chlorodibenzosuberane (41 g, 180 mmol, 1.2 eq), sodium iodide (2.2 g, 15 mmol, 0.1 eq) and triethylamine (63 mL, 450 mmol, 3.0 eq) in dioxane (300 mL) was stirred at 90° C. overnight. The reaction mixture was concentrated in vacuo and the residue was partitioned between ethyl acetate and water. The organic phase was washed with brine, dried over MgSO4, and concentrated. The crude product was passed through a silica gel plug, eluting with CH2Cl2. After concentration, the resulting solid was triturated with ether to yield 27 g (55%) of methyl 1-(10,11-dihydro5H-dibenzo[a,d][7]annulen-5-yl)-1,2,5,6-tetrahydropyridine-3-carboxylate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07595327B2
出典データセットuspto-grants-2009_09
ORD IDord-7faa392ab5ba428d8d9d7037bc35f0ee
出典メモuspto-grants-2009_09