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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 79135생성일: 2026년 10월 24일

Triethylamine → 1-(6-Bromo-3-pyridazinyl)-N,N-dimethyl-4-piperidinamine

https://huagongshe.com/ko/reaction/79135

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물3,6-DibromopyridazineHCID 248852—
반응물N,N-Dimethylpiperidin-4-amineHCID 417391—
용매TetrahydrofuranHCID 8028—
생성물1-(6-Bromo-3-pyridazinyl)-N,N-dimethyl-4-piperidinamineHCID 5829993289.8%

반응 조건

온도70 °C

반응 단계

N,N-dimethylpiperidin-4-amine (0.505 g, 3.94 mmol), 3,6-dibromopyridazine (0.511 g, 2.15 mmol), and triethylamine (0.599 mL, 4.30 mmol) were combined in 5 mL of THF. The solution was heated at 70° C. for 17 hours. The solution was cooled to room temperature and then purified on CombiFlash column (dry loaded), eluting with 10% methanol/0.5% NH4OH (˜28% in water)/DCM isocratic. The fractions containing the product were combined and concentrated under vacuum to give compound 201 (0.550 g, 89.8% yield) as an off white solid. 1H NMR (500 MHz, MeOD-d3) δ 7.51 (1 H, d, J=9.8 Hz), 7.24 (1 H, d, J=9.8 Hz), 4.45 (2 H, d, J=13.7 Hz), 2.98 (2 H, td, J=13.0, 2.2 Hz), 2.61 (1 H, tt, J=11.5, 3.8 Hz), 2.38 (6 H, s), 1.99-2.07 (2 H, m), 1.45-1.58 (2 H, m, J=12.5, 12.2, 12.2, 4.2 Hz) ppm; LCMS-ESI (POS), M/Z, M+1: Found 285.0.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841312B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-b228a14ea9f1475f8633466dd31bf50a
출처 메모uspto-grants-2014_09