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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 524946생성일: 2026년 10월 24일

Triphenylphosphine → 3'-Methyl-[4,4'-bipyridin]-3-amine

https://huagongshe.com/ko/reaction/524946

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물Potassium Phosphate, TribasicHCID 62657—
반응물4-Bromo-3-methylpyridineHCID 428351—
반응물(3-((tert-Butoxycarbonyl)amino)pyridin-4-yl)boronic acidHCID 15366412—
촉매PalladiumHCID 23938—
용매1,4-DioxaneHCID 31275—
생성물3'-Methyl-[4,4'-bipyridin]-3-amineHCID 83167784—

반응 단계

[3-(tert-butoxycarbonylamino)-4-pyridyl]boronic acid (100 mg, 0.4201 mmol), palladium; triphenylphosphane (48.55 mg, 0.04201 mmol), 4-bromo-3-methyl-pyridine (113.9 mg, 0.5461 mmol), K3PO4 (630.0 μL of 2 M, 1.260 mmol), in dioxane (4.000 mL) was heated at 130° C. for 30 min in a MW. The reaction mixture was partitioned between water and DCM. Combined organic extract was dried and concentrated in vacuo. The residue was dissolved in DCM (10 mL) and TFA (2 mL) was added. After 1 h, the reaction mixture was concentrated in vacuo. The residue was loaded on a SCX column, washed with MeOH. The product was eluted with a 2M NH3 in MeOH., filtrate was concentrated in vacuo yielding 3′-methyl-[4,4′-bipyridin]-3-amine that was used in next reaction w/o further purification (90 mg). MS (ES+) 172.1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09340546B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-0eacb3f7f5ae4292b652bcf623f15182
출처 메모uspto-grants-2016_05