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HRID 867675作成日:2026年10月25日

Sodium hydride → 1-[3-(Dimethylamino)propyl]-3-(1-methyl-4-piperidinyl)-1H-indazole difumarate

https://huagongshe.com/reaction/867675

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物3-Chloro-N,N-dimethyl-1-propanamineHCID 66960—
反応物Fumaric AcidHCID 444972—
反応物HCID 178480237HCID 178480237—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
溶媒DimethylformamideHCID 6228—
溶媒AcetonitrileHCID 6342—
生成物1-[3-(Dimethylamino)propyl]-3-(1-methyl-4-piperidinyl)-1H-indazole difumarateHCID 1403250318.7%

反応手順

To a stirred suspension of 1.15 g of sodium hydride (50% oil dispersion) in 30 ml of dimethylformamide, under nitrogen, was added dropwise 4.3 g of 3-(1-methyl-4-piperidinyl)-1H-indazole dissolved in 30 ml of hot dimethylformamide. After stirring at ambient temperature for 1 hr, a solution of 3.3 g of dimethylaminopropylchloride in 30 ml of toluene was added dropwise. The reaction was then heated at 60° for 1 hr and then stirred at ambient temperature for 16 hrs. The reaction mixture was poured into water and the aqueous suspension was extracted with ethyl acetate (3×150 ml). The organic extracts were combined, washed with water, brine, dried over anhydrous magnesium sulfate, and the solvent evaporated in vacuo to yield an oil. The oil was dissolved in 25 ml of acetonitrile and 4.6 g of fumaric acid was added. The mixture was warmed on the steam bath (ca. 15 min), and then left at ambient temperature for 15 hrs. The resultant solid was filtered and recrystallized from dimethylformamide (thrice) with cooling (ca. 5°) to yield 1.4 g (18.7%) of product, mp 161°-163° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04775761
出典データセットuspto-grants-1988_10
ORD IDord-8d8a4f42e31d4a9eb1a6020fc7ca8dc6
出典メモuspto-grants-1988_10