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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2064967생성일: 2026년 10월 25일

Nitrogen → 2-(2-Methyl-[1,3]dioxolan-2-yl)-6-(4-nitro-pyrazol-1-ylmethyl)-pyridine

https://huagongshe.com/reaction/2064967

반응식

참여 물질

역할이름HCID투입량
반응물NitrogenHCID 947—
반응물Potassium CarbonateHCID 11430—
반응물4-nitro-1H-pyrazoleHCID 16376—
반응물Iodide IonHCID 30165—
반응물Methanesulfonic acid 6-(2-methyl-[1,3]dioxolan-2-yl)-pyridin-2-ylmethyl esterHCID 86649482—
용매AcetoneHCID 180—
생성물2-(2-Methyl-[1,3]dioxolan-2-yl)-6-(4-nitro-pyrazol-1-ylmethyl)-pyridineHCID 66928936—

반응 단계

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a solution of methanesulfonic acid 6-(2-methyl-[1,3]dioxolan-2-yl)-pyridin-2-ylmethyl ester (273 mg, 1.00 mmol) in acetone (4.0 mL) was added, under inert atmosphere (N2) to a solution of 4-nitro-1H-pyrazole (115 mg, 1.00 mmol) in acetone (4.0 mL). K2CO3 (698 mg, 5.00 mmol) and TBA iodide (64 mg, 0.20 mmol) were added and the reaction mixture was stirred at rt for 5 h. The solvent was removed under reduced pressure. Water (10 mL) and EA (10 mL) were added. The aq. layer was extracted with EA (10 mL) and the combined org. extracts were dried over Na2SO4, filtered, and the solvents were removed under reduced pressure. Purification of the residue by FC (30:10 to 50:50 hept-EA) gave the title compound as a pale yellow oil. LC-MS-conditions 02: tR=0.87 min; [M+H]+=291.27.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08288419B2
출처 데이터셋uspto-grants-2012_10
ORD IDord-c16fb77f6c534b768e0753b8fdedaa8e
출처 메모uspto-grants-2012_10