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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 920124생성일: 2026년 10월 26일

Dimethylformamide → tert-butyl N-(4-fluoro-3-formylpyridin-2-yl)carbamate

https://huagongshe.com/reaction/920124

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물tert-butyl N-(4-fluoropyridin-2-yl)carbamateHCID 51354888—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물tert-butyl N-(4-fluoro-3-formylpyridin-2-yl)carbamateHCID 8967023957%

반응 단계

To a stirred solution of tert-butyl 4-fluoropyridin-2-ylcarbamate (1 g, 4.72 mmol) in THF (20 mL) was added dropwise n-BuLi (4.7 mL, 11.8 mmol) at −78° C. After stirring for 0.5 h, a solution of DMF (2 mL) in THF (2 mL) was added dropwise at −78° C. TLC indicated the reaction was completed. The reaction was quenched with 1N HCl at −78° C. to pH=4. Then water (20 mL) was added and extracted with ethyl acetate (3×20 mL). The combined organic phase was washed with brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by column chromatography (EtOAc:PE=1:2) to give the title compound (0.65 g, 57%) as a white solid. 1H-NMR (600 MHz, DMSO-d6) δ 10.35 (s, 1H), 9.99 (s, 1H), 8.58-8.56 (m, 1H), 7.23-7.21 (m, 1H), 1.46 (s, 9H) ppm.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09273046B2
출처 데이터셋uspto-grants-2016_03
ORD IDord-076440773d67442988b85b120393a049
출처 메모uspto-grants-2016_03