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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 447317생성일: 2026년 10월 26일

1-Bromo-4-iodobenzene → 1-(4-Bromophenyl)-cis-3,5-dimethylpiperazine

https://huagongshe.com/reaction/447317

반응식

참여 물질

역할이름HCID투입량
반응물1-Bromo-4-iodobenzeneHCID 11522—
반응물BinolHCID 11762—
반응물Potassium Phosphate, TribasicHCID 62657—
반응물rel-(2R,6S)-2,6-dimethylpiperazineHCID 6950261—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물1-(4-Bromophenyl)-cis-3,5-dimethylpiperazineHCID 6673036160.2%

반응 단계

A microwave vial was charged with 1-bromo-4-iodobenzene (1.0 g, 3.5 mmol), CuI (0.135 g, 0.707 mmol), BINOL (0.202 g, 0.707 mmol), and K3PO4 (1.5 g. 7.1 mmol). The vial was capped and then evacuated and backfilled with Ar. Cis-2,6-dimethylpiperazine (0.605 g, 5.30 mmol) and DMF (4 mL) were then added. The resulting mixture was stirred at rt for 4 d. The mixture was diluted with EtOAc, filtered through a cake of Celite and the filtrate was concentrated to give the crude product. Crude product was purified by flash chromatography using MeOH/CH2Cl2 (2:98 to 15:85) to give the title compound as a red solid (567 mg, 59%). 1H NMR (400 MHz, MeOD) δ 7.33 (d, J=8.8 Hz, 2H), 6.89 (d, J=8.8 Hz, 2H), 3.63-3.60 (m, 2H), 3.18-3.07 (m, 2H), 2.40 (t, J=11.6 Hz, 2H), 1.23 (d, J=6.4 Hz, 6H); MS ESI 269.0 [M+H]+, calcd for [C12H17BrN2+H]+ 269.06.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08481533B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-c652735f6b6d4920a38ce1c2f3fd31a9
출처 메모uspto-grants-2013_07