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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 867675생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/867675

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물3-Chloro-N,N-dimethyl-1-propanamineHCID 66960—
반응물Fumaric AcidHCID 444972—
반응물HCID 178480237HCID 178480237—
용매WaterHCID 962—
용매TolueneHCID 1140—
용매DimethylformamideHCID 6228—
용매AcetonitrileHCID 6342—
생성물1-[3-(Dimethylamino)propyl]-3-(1-methyl-4-piperidinyl)-1H-indazole difumarateHCID 1403250318.7%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04775761
출처 데이터셋uspto-grants-1988_10
ORD IDord-8d8a4f42e31d4a9eb1a6020fc7ca8dc6
출처 메모uspto-grants-1988_10