돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 719생성일: 2026년 10월 23일

1-Methylpiperazine → Methyl 3-(4-methyl-1-piperazinyl)-5-nitrobenzoate

https://huagongshe.com/ko/reaction/719

반응식

참여 물질

역할이름HCID투입량
반응물1-MethylpiperazineHCID 53167—
반응물Methyl 3-bromo-5-nitrobenzoateHCID 239341—
시약Cesium carbonateHCID 10796—
촉매1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매1,4-DioxaneHCID 31275—
생성물Methyl 3-(4-methyl-1-piperazinyl)-5-nitrobenzoateHCID 6751362865.18%

반응 조건

온도110 °C

반응 단계

To the stirred suspension ofmethyl 3-bromo-5-nitrobenzoate (2 g, 7.69 mmol) , cesium carbonate (12.53 g, 38.46 mmol) and (9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) (0.111 g, 0.19 mmol) in Dioxane (12 mL) (degassed with N2) was added pd (dba)3 (0.176 g, 0.19 mmol) and cesium carbonate (12.53 g, 38.46 mmol) AND rxn was heated at 110 ºC for 1 hr in microwaved. LCMS showed the m+1= 280. The crude raection mixture was filtered over celite. The filtrate was concentarted. The crude solid was diluted by 20 mL ethyl acetate, washed with 3x10 mL water, brine, collected the organic layers, concentrated. The crude solid was added to a silica gel column and was eluted with 0-10% methanol in DCM. Collected desired fractions. Obtained=1.4 gm. 1H NMR (300 MHz, DICHLOROMETHANE- _d_ 2) d ppm 2.32 (s, 3 H) 2.43 - 2.64 (m, 4 H) 3.13 - 3.40 (m, 4 H) 3.93 (s, 3 H) 7.85 (d, _J_ =1.70 Hz, 2H) 8.18 (t, _J_ =1.60 Hz, 1 H) Registered as AZ13477915.

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-0986b91ec7734959810ebeac46571d3f
출처 메모750 AstraZeneca ELN dataset