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HRID 724475생성일: 2026년 10월 25일

5-Butyl-pyridine-2-carboxylic acid methoxy-methyl-amide → 1-(5-Butyl-pyridin-2-yl)-ethanone

https://huagongshe.com/reaction/724475

반응식

참여 물질

역할이름HCID투입량
반응물5-Butyl-pyridine-2-carboxylic acid methoxy-methyl-amideHCID 58747007—
반응물HCID 178418689HCID 178418689—
용매TetrahydrofuranHCID 8028—
생성물1-(5-Butyl-pyridin-2-yl)-ethanoneHCID 1243628696.9%

반응 단계

MeMgBr (1.98 ml, 5.94 mmol) was added to a solution of 5-butyl-pyridine-2-carboxylic acid methoxy-methyl-amide (I-2A-38a; 880 mg, 3.96 mmol) in THF (10 ml) at 0° C. The reaction mixture was allowed to warm to room temperature and was stirred for 1.5 h, quenched with saturated aqueous NH4Cl (1 ml), and saturated aqueous NaCl. The aqueous THF solution was extracted with EtOAc (2×), and the combined organic extracts were washed with saturated aqueous NaCl, dried, and concentrated under vacuum to yield the product I-2A-38b as an oil (680 mg): APcl MS 178.1 (M+1)+; 1H NMR (400 MHz, CDCl3) δ 8.47 (d, 1H, J=1.6 Hz), 7.95 (d, 1H, J=8.3 Hz), 7.60 (dd, 1H, J=1.6, 8.3 Hz), 2.69 (s, 3H), 2.67 (t, 2H, J=7.9 Hz), 1.65–1.56 (m, 2H), 1.40–1.30 (m, 2H), 0.92 (t, 3H, J=7.4 Hz).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07141669B2
출처 데이터셋uspto-grants-2006_11
ORD IDord-ef26b15e9b644253a18e4f056967d605
출처 메모uspto-grants-2006_11