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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 77609생성일: 2026년 10월 24일

1,2-Dichloroethane → 4-(2-(Bis(isoquinolin-1-ylmethyl)amino)ethyl)benzenesulfonamide

https://huagongshe.com/ko/reaction/77609

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DichloroethaneHCID 11—
반응물Acetic AcidHCID 176—
반응물4-(2-Aminoethyl)benzenesulfonamideHCID 169682—
반응물Isoquinoline-1-carbaldehydeHCID 265306—
반응물Sodium triacetoxyborohydrideHCID 5049666—
용매WaterHCID 962—
생성물4-(2-(Bis(isoquinolin-1-ylmethyl)amino)ethyl)benzenesulfonamideHCID 4623392477%

반응 조건

온도0 °C

반응 단계

A solution of 4-(2-aminoethyl)benzenesulfonamide (1.0 g, 5.0 mmol), AcOH (1.0 mL) and isoquinoline-1-carbaldehyde (2.09 g, 13.3 mmol) in DCE (50 mL) was stirred at 75° C. for 30 min under nitrogen. The reaction mixture was cooled to 0° C., and treated with NaBH(OAc)3 (3.165 g, 15 mmol). The reaction mixture was stirred at room temperature for overnight and decomposed with water. The reaction mixture was extracted with DCM. The organic layer was dried and concentrated under reduced pressure. The residue was purified by flash chromatography over silica gel to afford 4-(2-(bis(isoquinolin-1-ylmethyl)amino)ethyl)benzenesulfonamide (1.86 g, 77%). 1H NMR (400 MHz, DMSO-d6) 8.24 (d, J=8.8 Hz, 2H), 7.96 (d, J=8.4 Hz, 2H), 7.91 (d, J=8.0 Hz, 2H), 7.72 (t, J=7.8 Hz, 2H), 7.65 (d, J=8.4 Hz, 2H), 7.55 (t, J=7.6 Hz, 2H), 7.50 (d, J=8.4 Hz, 2H), 7.30 (d, J=6.0 Hz, 2H), 7.29 (s, 2H), 4.01 (s, 4H), 2.94 (t, J=7.0 Hz, 2H), 2.78 (t, J=7.0 Hz, 2H); MS (ESI), 483.3 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08840865B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-4f2b5319bf4d4c6f82f673305615a567
출처 메모uspto-grants-2014_09