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HRID 72708作成日:2026年10月24日

Azetidine → 4-(Azetidin-1-yl)-6-chloropyrimidine-5-carbaldehyde

https://huagongshe.com/ja/reaction/72708

反応式

関与物質

役割名称HCID仕込み量
反応物AzetidineHCID 10422—
反応物4,6-Dichloro-5-pyrimidinecarbaldehydeHCID 819691—
触媒TriethylamineHCID 8471—
溶媒ChloroformHCID 6212—
生成物4-(Azetidin-1-yl)-6-chloropyrimidine-5-carbaldehydeHCID 86712562—

反応手順

To a solution of 4,6-dichloropyrimidine-5-carbaldehyde (1.00 g, 5.65 mmol) in chloroform at 0° C. were added azetidine (99%, 0.392 mL, 5.71 mmol) and triethylamine (5 drops). The reaction mixture was allowed to warm to room temperature and then stirred for 18 hours. The reaction mixture was filtered, and the filtrate was purified by silica gel chromatography (Gradient: 0% to 100% ethyl acetate in heptane) to provide the product. Yield: 880 mg, 4.45 mmol, 79%. LCMS m/z 198.1, 200.1 (M+1). 1H NMR (400 MHz, CD3OD) δ 2.34-2.43 (m, 2H), 4.12-4.33 (br m, 4H), 8.30 (s, 1H), 10.28 (s, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08829010B2
出典データセットuspto-grants-2014_09
ORD IDord-50b2e28456f84a5494615235ad31a5bc
出典メモuspto-grants-2014_09