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HRID 22471作成日:2026年10月25日

Diethyl Ether → 1-[3-(Dimethylamino)propyl]-3-phenyl-1H-pyrazolo[4,3-c]pyridine dihydrochloride

https://huagongshe.com/reaction/22471

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl EtherHCID 3283—
反応物Sodium hydrideHCID 24758—
反応物3-Chloro-N,N-dimethyl-1-propanamineHCID 66960—
反応物3-Phenyl-1H-pyrazolo[4,3-c]pyridineHCID 13801125—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物1-[3-(Dimethylamino)propyl]-3-phenyl-1H-pyrazolo[4,3-c]pyridine dihydrochlorideHCID 19930480—

反応手順

3-Phenyl-1H-pyrazolo[4,3-c]pyridine (3.90 g) was suspended in 50 ml of dimethylformamide and 60% NaH (1.0 g) was added. After stirring for 90 minutes, dimethylaminopropyl chloride (3.0 g) was added, and stirring was continued for 1 hour. At the end of this time the reaction was warmed to 55° and, after an additional 2 hours, an additional 0.50 g of dimethylaminopropyl chloride was added. Warming and stirring was continued for 1 hour, after which time the reaction mixture was distributed between ether and H2O. The organic phase was dried, evaporated, and purified by flash chromatography (5% triethylamine-ethyl acetate), giving an oil upon evaporation of the product-containing fractions. The hydrochloride was formed in ethereal HCl and recrystallized from methanol-ether to give 3.76 g of product, m.p. 237°-239°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05428169
出典データセットuspto-grants-1995_06
ORD IDord-4913146aa9ce408792d93d92a3809610
出典メモuspto-grants-1995_06