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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 704824생성일: 2026년 10월 26일

Isopropylamine → [6-(dimethylamino)hexyl]-4,5-diphenyl-1H-pyrazole-1-acetamide

https://huagongshe.com/reaction/704824

반응식

참여 물질

역할이름HCID투입량
반응물IsopropylamineHCID 6363—
반응물DiisopropylethylamineHCID 81531—
반응물6-(Dimethylamino)hexylamineHCID 258544—
반응물4,5-Diphenyl-1-(ethoxycarbonylmethyl)-pyrazoleHCID 14699551—
용매Diethyl EtherHCID 3283—
용매ChloroformHCID 6212—
생성물[6-(dimethylamino)hexyl]-4,5-diphenyl-1H-pyrazole-1-acetamideHCID 86743406—

반응 단계

A mixture of 8 g (0.026 mol) of ethyl 4,5-diphenyl-1H-pyrazole-1-acetate of Example 1, 4.1 g (0.028 mol) of dimethylaminohexylamine and 33.3 mL (0.19 mol) of diisopropylethylamine was stirred on a steam bath under nitrogen for 18 hours. Thin layer chromatography on silica gel with 5% isopropylamine in chloroform showed incomplete reaction. Another 1 mL of dimethylaminohexylamine was added and stirring continued on a steam bath for an additional 24 hours. The reaction was stripped in vacuo, taken up in 200 mL of ether, washed two times with water, washed once with half saturated sodium bicarbonate solution, washed with water again, washed with saturated sodium chloride solution, dried over magnesium sulfate, treated with decolorizing carbon, filtered and stripped. The residue was taken up in ether and treated with a slight excess of hydrochloric acid. The hydrochloride salt was extracted into water and washed three times with ether; the water layer was chilled, and made basic with solid sodium carbonate and extracted two times with ether. The ether extracts were combined, washed once with saturated sodium chloride, dried over magnesium sulfate, treated with decolorizing carbon, filtered and stripped. The resulting residue was triturated in pentane to yield 4.14 g of N-([6-(dimethylamino)hexyl]-4,5-diphenyl-1H-pyrazole-1-acetamide, mp 60°-63° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04988725
출처 데이터셋uspto-grants-1991_01
ORD IDord-0bc021e3ff9f4c52a05e235ade8baba8
출처 메모uspto-grants-1991_01