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HRID 416224作成日:2026年10月27日

Acetylpyrazine → (E)-3-(Dimethylamino)-1-(pyrazin-2-YL)prop-2-EN-1-one

https://huagongshe.com/reaction/416224

反応式

関与物質

役割名称HCID仕込み量
反応物AcetylpyrazineHCID 30914—
反応物Dimethylformamide dimethyl acetalHCID 78373—
溶媒TriethylamineHCID 8471—
溶媒tert-Butyl methyl etherHCID 15413—
生成物(E)-3-(Dimethylamino)-1-(pyrazin-2-YL)prop-2-EN-1-oneHCID 582535481.4%

反応手順

A solution of acetylpyrazine (5 g, 40.9 mmol) in N,N-dimethylformamide dimethyl acetal (10.9 mL, 81.8 mmol) and Et3N (5.7 mL) was heated at 110° C. for 16 h. The heating was stopped and a precipitate was formed while it was allowed to cool down to room temperature. The suspension was diluted with tert-butyl methyl ether; the solid was separated by filtration and washed with tert-butyl methyl ether. This material was triturated with the same solvent, filtered off and dried to afford the title compound 23a as a yellow solid (5.9 g, 33.3 mmol, 81% yield). 1H NMR (400 MHz, DMSO-d6) δ (ppm): 9.09 (s, 1H), 8.73 (d, J=2.4 Hz, 1H), 8.66 (dd, J=2.4, 1.6 Hz, 1H), 7.84 (d, J=12.4 Hz, 1H), 6.30-6.20 (m, 1H), 3.19 (s, 3H), 2.93 (s, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08088805B2
出典データセットuspto-grants-2012_01
ORD IDord-fc1dd4dd780c44d7b0412d37f347e4b9
出典メモuspto-grants-2012_01