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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2121639생성일: 2026년 10월 24일

Potassium Carbonate → 2,2-dimethyl-N-(2-methyl-4-pyrrolidin-1-yl-quinolin-7-yl)-propionamide

https://huagongshe.com/ko/reaction/2121639

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물TrimethylacetamideHCID 12957—
반응물7-iodo-2-methyl-4-pyrrolidin-1-yl-quinolineHCID 11336663—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매DimethylformamideHCID 6228—
생성물2,2-dimethyl-N-(2-methyl-4-pyrrolidin-1-yl-quinolin-7-yl)-propionamideHCID 1017187856.2%

반응 조건

온도150 °C

반응 단계

A suspension of 0.338 mg (1 mmol) of 7-iodo-2-methyl-4-pyrrolidin-1-yl-quinoline, 0.81 g (8 mmol) of trimethylacetamide, 0.414 g (3 mmol) of potassium carbonate (water free) and 20 mg (0.1 mmol) of copper (I) iodide in DMF (10 ml) was heated at 150° C. (oil bath temperature) under an argon atmosphere for 20 h. The reaction mixture was partitioned between EtOAc and water, the layers were separated, the organic layer washed twice with water dried over sodium sulphate and concentrated in vacuo. The residue was applied to silica gel column with CH2Cl2/MeOH/NH4OH (20:1:0.2) as eluent. Combination of the purified fractions and concentration in vacuo gave 175 mg (50.4%) of the desired 2,2-dimethyl-N-(2-methyl-4-pyrrolidin-1-yl-quinolin-7-yl)-propionamide as light brown solid. ISP mass spectrum, m/e: 312.3 (M+1 calculated for C19H25N3O: 312).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06696467B2
출처 데이터셋uspto-grants-2004_02
ORD IDord-c4b1cd38468c4edd8800f4d292a87e9e
출처 메모uspto-grants-2004_02