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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 130415생성일: 2026년 10월 24일

Triethylamine → 4-(cis-3,5-Dimethyl-1-piperazinyl)-2-nitrobenzonitrile

https://huagongshe.com/ko/reaction/130415

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물4-Chloro-2-nitrobenzonitrileHCID 96924—
반응물rel-(2R,6S)-2,6-dimethylpiperazineHCID 6950261—
반응물Sodium MethoxideHCID 10942334—
촉매2-(2'-Di-tert-butylphosphine)biphenylpalladium(II) acetateHCID 11982262—
생성물4-(cis-3,5-Dimethyl-1-piperazinyl)-2-nitrobenzonitrileHCID 69198156—

반응 조건

온도85 °C

반응 단계

A mixture of 4-chloro-2-nitrobenzonitrile (Tetrahedron 1994, 50, 5515-5126) (650 mg, 3.56 mmol), sodium methoxide (270 mg, 5.00 mmol) and acetato-(2′-di-tert-butylphosphino-1,1′-biphenyl-2-yl)palladium (II) (115 mg, 0.25 mmol) was treated with triethylamine (0.25 ml, 1.79 mmol) followed by cis-2,6-dimethylpiperazine (488 mg, 4.27 mmol) and the mixture heated to 85° C. under an inert atmosphere over 30 minutes. The mixture was then kept at this temperature for 16 hours. The mixture was then filtered through kieselguhr, washing with toluene (50 ml) and the filtrate reduced in vacuo. The residue was then purified using an SCX ion exchange cartridge (Varian bond-elute) eluting with methanol followed by 2M ammonia in methanol to afford a dark residue which was purified by mass directed autoprep BPLC to afford the title compound as the formic acid salt. MS (ES+) m/e 261 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07381728B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-c9f26323c77a4bdebefe7106d812054a
출처 메모uspto-grants-2008_06