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HRID 17120作成日:2026年10月26日

Triethylamine → Tert-butyl (2e)-3-[4-amino-3-(4-phenoxyphenyl)thieno[3,2-c]pyridin-7-yl]acrylate

https://huagongshe.com/reaction/17120

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物tert-Butyl acrylateHCID 15458—
反応物7-Iodo-3-(4-phenoxyphenyl)thieno[3,2-c]pyridin-4-amineHCID 18450878—
溶媒DimethylformamideHCID 6228—
生成物Tert-butyl (2e)-3-[4-amino-3-(4-phenoxyphenyl)thieno[3,2-c]pyridin-7-yl]acrylateHCID 6977650561%

反応条件

温度80 °C

反応手順

A mixture of Example 10B (0.417 g, 0.94 mmol), tert-butyl acrylate (0.26 mL, 1.74 mol) and triethylamine (0.7 mL, 5 mmol) in DMF (3 mL) was degassed with nitrogen for 45 minutes, treated with PdCl2(o-tol3P)2 (0.032 g, 0.046 mmol), and heated to 80° C. overnight. The resulting mixture was cooled to room temperature, then partitioned between water and ethyl acetate. The organic extract was washed with brine, dried (Na2SO4), filtered, and concentrated. The residue was purified by flash column chromatography on silica gel with 30% ethyl acetate/hexanes to provide 0.25 g (61% yield) of the desired product. MS (ESI(+)) m/e 445 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07737160B2
出典データセットuspto-grants-2010_06
ORD IDord-a44de1ab0f524337ae9a40101dba9e91
出典メモuspto-grants-2010_06