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HRID 9193作成日:2026年10月25日

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

https://huagongshe.com/reaction/9193

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-Dibromo-1,1,2,2-tetrachloroethaneHCID 69426—
反応物2-Methoxypyrazolo[1,5-a]pyridineHCID 12284427—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
溶媒HexaneHCID 8058—
生成物7-Bromo-2-methoxypyrazolo[1,5-a]pyridineHCID 2198465864.8%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07091215B2
出典データセットuspto-grants-2006_08
ORD IDord-0fcd62becadc4836ba07d9659cf62752
出典メモuspto-grants-2006_08