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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 230682생성일: 2026년 10월 24일

N,N-Dimethylglycine → 1-methyl-5-{4-[3-(trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazol-1-yl]phenyl}-2-pyrrolidinone

https://huagongshe.com/ko/reaction/230682

반응식

참여 물질

역할이름HCID투입량
반응물N,N-DimethylglycineHCID 673—
반응물Potassium CarbonateHCID 11430—
반응물3-(Trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazoleHCID 2802863—
반응물5-(4-Bromophenyl)-1-methyl-2-pyrrolidinoneHCID 57762794—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매Dimethyl SulfoxideHCID 679—
생성물1-methyl-5-{4-[3-(trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazol-1-yl]phenyl}-2-pyrrolidinoneHCID 248259097%

반응 조건

온도180 °C

반응 단계

A mixture of 5-(4-bromophenyl)-1-methyl-2-pyrrolidinone (141 mg, 0.56 mmol), 3-(trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazole (111 mg, 0.58 mmol), copper (I) iodide (10 mol %, 11 mg, 0.06 mmol), N,N-dimethylglycine (20 mol %, 12 mg, 0.12 mmol) and potassium carbonate (162 mg, 1.17 mmol) in dimethylsulfoxide (3 ml) was stirred at 180° C. in a microwave reactor for a total of 2 h. The reaction mix was filtered through a 5 g pre-packed silica column washing through with dichloromethane (20 ml), the filtrate was washed with water (50 ml) and the organic layer dried over sodium sulphate. The solvent was removed by rotary evaporation and the sample purified by mass directed auto prep. The final product was partitioned between dichloromethane (3 ml) and water (3 ml). The organic layer was separated and solvent removed by rotary evaporation to give the title compound as a brown oil (14 mg, 7%)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07566735B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-efbdc9926752420788d19c0c91a3d1d7
출처 메모uspto-grants-2009_07