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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 9193생성일: 2026년 10월 24일

1,2-Dibromo-1,1,2,2-tetrachloroethane → 7-Bromo-2-methoxypyrazolo[1,5-a]pyridine

https://huagongshe.com/ko/reaction/9193

반응식

참여 물질

역할이름HCID투입량
반응물1,2-Dibromo-1,1,2,2-tetrachloroethaneHCID 69426—
반응물2-Methoxypyrazolo[1,5-a]pyridineHCID 12284427—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물7-Bromo-2-methoxypyrazolo[1,5-a]pyridineHCID 2198465864.8%

반응 단계

A solution of 2-methoxypyrazolo[1,5-a]pyridine (7.15 g) [CAS No.59942-88-0] in tetrahydrofuran (140 mL) was cooled to −78° C. under a nitrogen stream, and then a solution of n-butyllithium in hexane (1.6 M; 46 mL) was added dropwise and the mixture was stirred for 30 minutes. A solution of 1,2-dibromo-1,1,2,2-tetrachloroethane (18.9 g) in tetrahydrofuran (30 mL) was added dropwise at −78° C., and stirring was continued for 1 hour. After increasing the temperature of the reaction mixture to room temperature and adding water, extraction was performed with ethyl acetate and the extract was washed with brine. After drying the obtained organic layer over anhydrous magnesium sulfate and filtering it, the solvent was concentrated under reduced pressure, the residue was purified by silica gel column chromatography, and the title compound (7.1 g) was obtained from the n-hexane:ethyl acetate (50:1) fraction as a yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091215B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-0fcd62becadc4836ba07d9659cf62752
출처 메모uspto-grants-2006_08