戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 347845作成日:2026年10月27日

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

https://huagongshe.com/reaction/347845

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-DiiodoethaneHCID 12224—
反応物Ammonium ChlorideHCID 25517—
反応物tert-butyl N-[2-methylthiopyrazolo[1,5-a]pyridin-3-yl]carbamateHCID 21984591—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物tert-Butyl N-[7-iodo-2-methylthiopyrazolo[1,5-a]pyridin-3-yl]carbamateHCID 2198451168.6%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07176216B2
出典データセットuspto-grants-2007_02
ORD IDord-7ec69c56efe7422795afe34887b97bb3
出典メモuspto-grants-2007_02