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HRID 977926作成日:2026年10月27日

Triethylamine → Lomerizine Hydrochloride

https://huagongshe.com/reaction/977926

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Toluene, alpha-chloro-2,3,4-trimethoxy-HCID 97491—
反応物1-(Bis(4-fluorophenyl)methyl)piperazineHCID 152932—
溶媒BenzeneHCID 241—
生成物Lomerizine HydrochlorideHCID 12212598.5%

反応手順

1.3 g (6.0 millimoles) of 2,3,4-trimethoxybenzyl chloride [see Monatsh., 95 (3), 942 (1964)], 1.7 g (5.9 millimoles) of bis(4-fluorophenyl)methylpiperazine and 1.2 ml (8.6 millimoles) of triethylamine were heated under reflux for 6 hours in 50 ml of benzene. The reaction mixture was allowed to cool to room temperature, washed with water, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. A mixture of 2 ml of conc. hydrochloric acid and 20 ml of ethanol was added to the resulting oily product, and the mixture was concentrated under reduced pressure. Ether was added, and the precipitated crystals were collected by filtration. Recrystallization of the crystals from ethanol-ether gave 1.6 g of 1-(2,3,4-trimethoxybenzyl)-4-[bis(4-fluorophenyl)methyl]piperazine dihydrochloride as colorless crystals. The product showed the same property values as the compound obtained in Example 4.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04663325
出典データセットuspto-grants-1987_05
ORD IDord-d166fb5bb6d94b9793f7aadc19477feb
出典メモuspto-grants-1987_05