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HRID 1782580생성일: 2026년 10월 25일

3,5-Dibromo-4-methylpyridin-2-amine → 3-Bromo-4-methylpyridin-2-amine

https://huagongshe.com/reaction/1782580

반응식

참여 물질

역할이름HCID투입량
반응물3,5-Dibromo-4-methylpyridin-2-amineHCID 817683—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물3-Bromo-4-methylpyridin-2-amineHCID 1441804371%

반응 조건

온도-78 °C

반응 단계

To a solution of 3,5-dibromo-4-methyl-pyridin-2-ylamine (3.38 g, 12.7 mmol) in THF (60 mL) cooled to −78° C. was added n-BuLi (1.9M in pentane) (13.4 mL, 25.4 mmol) to give an orange solution. The solution was stirred at −78° C. for 1 h and then quenched with water (10 mL). The pH of the mixture was adjusted to ˜12 with 10N NaOH and then extracted with CH2Cl2 (3×30 mL), dried (Na2SO4), filtered and concentrated in vacuo to give an orange oil. Purification by column chromatography on silica gel (Et2O) afforded 3-bromo-4-methyl-pyridin-2-ylamine (1.68 g, 71%) as a pale yellow solid. 1H NMR (CDCl3) δ 2.32 (s, 3H), 5.00 (br s, 2H), 6.52 (d, 1H, J=6.0 Hz), 7.84 (d, 1H, J=6.0 Hz).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07498346B2
출처 데이터셋uspto-grants-2009_03
ORD IDord-66b8ab9f484d48448421cd75e67fabc9
출처 메모uspto-grants-2009_03