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HRID 1864994생성일: 2026년 10월 26일

1,2-Diiodoethane → tert-Butyl N-[7-iodo-2-methylthiopyrazolo[1,5-a]pyridin-3-yl]carbamate

https://huagongshe.com/reaction/1864994

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DiiodoethaneHCID 12224—
반응물Ammonium ChlorideHCID 25517—
반응물tert-butyl N-[2-methylthiopyrazolo[1,5-a]pyridin-3-yl]carbamateHCID 21984591—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물tert-Butyl N-[7-iodo-2-methylthiopyrazolo[1,5-a]pyridin-3-yl]carbamateHCID 21984511—

반응 단계

After dissolving tert-butyl N-[2-methylthiopyrazolo[1,5-a]pyridin-3-yl]carbamate (21.6 g) in tetrahydrofuran (1 L), a solution of n-butyllithium in hexane (1.6 M; 130 mL) was added dropwise at −78° C. under a nitrogen stream, and the mixture was stirred for 30 minutes. A solution of 1,2-diiodoethane (24 g) in tetrahydrofuran (50 mL) was added to the reaction mixture, and stirring was continued for 1 hour. Saturated aqueous ammonium chloride was added to the reaction mixture, the temperature was raised to room temperature, extraction was performed with ethyl acetate and the extract washed with water and brine. After drying over anhydrous magnesium sulfate and filtration, the solvent was concentrated under reduced pressure, the residue was purified by silica gel column chromatography, and the title compound was obtained from the n-hexane:ethyl acetate (5:1) fraction as yellow crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07625925B2
출처 데이터셋uspto-grants-2009_12
ORD IDord-c0f3c57000f54c5987577ce352c9f70c
출처 메모uspto-grants-2009_12