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HRID 451511作成日:2026年10月27日

Diisopropylethylamine → tert-Butyl 1-(2-(trifluoromethyl)pyridin-4-yl)piperidin-4-ylcarbamate

https://huagongshe.com/reaction/451511

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物4-Amino-1-Boc-piperidineHCID 1268291—
反応物4-Iodo-2-(trifluoromethyl)pyridineHCID 23436940—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物tert-Butyl 1-(2-(trifluoromethyl)pyridin-4-yl)piperidin-4-ylcarbamateHCID 6734244976.4%

反応手順

To a mixture of 4-iodo-2-(trifluoromethyl)pyridine (356 mg, 1.3 mmol) and Boc-4-aminopiperidine (340 mg, 1.7 mmol) in NMP (2.6 mL) was added DIPEA (319 L, 1.83 mmol). Argon was bubbled through the cloudy solution for 5 minutes before the reaction mixture was heated in the microwave for 3×30 minutes to 150° C. The mixture was then poured into water and extracted with ethyl acetate. The combined organic phases were dried over sodium sulfate, filtered and evaporated. Purification by chromatography (silica gel, 50 g, 0 to 100% ethyl acetate in heptane) afforded the title compound (343 mg, 76%) as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08486967B2
出典データセットuspto-grants-2013_07
ORD IDord-97a5cba06aba46a4b17d85304e4b67f4
出典メモuspto-grants-2013_07