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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 692생성일: 2026년 10월 24일

tert-Butyl piperazine-1-carboxylate → Tert-butyl 4-(3-chloro-4-cyanophenyl)piperazine-1-carboxylate

https://huagongshe.com/ko/reaction/692

반응식

참여 물질

역할이름HCID투입량
반응물tert-Butyl piperazine-1-carboxylateHCID 143452—
반응물4-Bromo-2-chlorobenzonitrileHCID 7010420—
시약Cesium carbonateHCID 10796—
촉매Binap, (A+-)-HCID 634876—
촉매Palladium (II) acetateHCID 4144353—
용매TolueneHCID 1140—
생성물Tert-butyl 4-(3-chloro-4-cyanophenyl)piperazine-1-carboxylateHCID 5648197747.09%

반응 조건

온도80 °C

반응 단계

In a 250 mL round-bottomed dried flask , diacetoxypalladium (0.036 g, 0.16 mmol) was treated with 2,2'-bis(diphenylphosphino)-1,1'-binaphthyl (0.195 g, 0.31 mmol) under nitrogen in toluene (35 mL). The reaction was heated to 80 °C and was stirred for 10 min. To the flask was then added tert-butyl piperazine-1-carboxylate (0.602 g, 3.23 mmol), cesium carbonate (0.527 g, 1.62 mmol), potassium carbonate (0.447 g, 3.23 mmol) and 1,4,7,10,13,16-hexaoxacyclooctadecane (0.085 g, 0.32 mmol). The reaction was then treated with 4-bromo-2-chlorobenzonitrile (0.7 g, 3.23 mmol) and was allowed to stir at 80°C for 5 h. The mixture was then filtered over celite and celite was washed with heptanes. The mixture was condensed under reduced pressure and the crude material was purified on preparative HPLC MS using the short high pH shallow gradient method (Mobile phase: 50-70% B; A: H2O with 10 mM NH4CO3 and 0.375% NH4OH v/v, B: CH3CN, 10 min run) on XBridge Prep C18 OBD, 30x50 mm, 5 mm, Waters reverse phase column, to afford tert-butyl 4-(3-chloro-4-cyanophenyl)piperazine-1-carboxylate (0.490 g, 47.1 %) as a white solid.

출처 및 근거

출처 데이터셋750 AstraZeneca ELN dataset
ORD IDord-80eaa5d6e27d4cf78d75715b3843cadc
출처 메모750 AstraZeneca ELN dataset