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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 347845생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/347845

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—
생성물tert-Butyl N-[7-iodo-2-methylthiopyrazolo[1,5-a]pyridin-3-yl]carbamateHCID 2198451168.6%

반응 단계

To a solution of tert-butyl N-[2-methylthiopyrazolo[1,5-a]pyridin-3-yl]carbamate (21.6 g) dissolved in tetrahydrofuran (1 L) was n-butyllithium (1.6M hexane solution; 130 mL) dropwise at −78° C. under a nitrogen stream, and the reaction mixture was stirred for 30 minutes. A solution of 1,2-diiodoethane (24 g) in tetrahydrofuran (50 mL) was added to the obtained reaction mixture, and stirring was continued for 1 hour. After adding saturated aqueous ammonium chloride to the reaction mixture, the temperature was raised to room temperature, extraction was performed with ethyl acetate and the organic extract was washed with water and brine. The obtained organic extract was dried over anhydrous magnesium sulfate and filtered, the solvent was evaporated under reduced pressure, the residue was purified by silica gel column chromatography and the title compound (21.5 g) was obtained as yellow crystals from the n-hexane:ethyl acetate (5:1) fraction.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07176216B2
출처 데이터셋uspto-grants-2007_02
ORD IDord-7ec69c56efe7422795afe34887b97bb3
출처 메모uspto-grants-2007_02