戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1042260作成日:2026年10月27日

Sodium Carbonate → 4-(2,4-di-tert-butoxypyrimidin-5-yl)-7H-pyrrolo[2,3-d]pyrimidine

https://huagongshe.com/reaction/1042260

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物(2,4-Di-tert-butoxypyrimidin-5-yl)boronic acidHCID 2735950—
反応物7H-Pyrrolo(2,3-d)pyrimidine, 4-chloro-HCID 5356682—
触媒Tetrakis(triphenylphosphine)palladiumHCID 11979704—
溶媒WaterHCID 962—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物4-(2,4-di-tert-butoxypyrimidin-5-yl)-7H-pyrrolo[2,3-d]pyrimidineHCID 6872607172%

反応条件

温度80 °C

反応手順

2,4-Di-tert-butoxypyrimidin-5-ylboronic acid (17.5 g, 65.4 mmol), tetrakis(triphenylphosphine) palladium(0) (7.6 g, 6.54 mmol) and sodium carbonate (20.8 g, 196 mmol) were added to a solution of 4-chloro-7H-pyrrolo[2,3-d]pyrimidine (10 g, 65.4 mmol) in DME (400 mL) and water (150 mL). With vigorous stirring, the mixture was heated to 80° C. for 24 h. The reaction mixture was cooled to RT and poured into water (100 mL). The mixture was extracted with EtOAc (100 mL) twice. The combined organic layers were washed with brine, dried over Na2SO4, and concentrated to give the crude product. This was purified by flash chromatography to give 4-(2,4-di-tert-butoxypyrimidin-5-yl)-7H-pyrrolo[2,3-d]pyrimidine (16.0 g, 72%) as a yellow solid. MS (APCI, pos. ion) m/z: 342.1 [M+H]+

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08557830B2
出典データセットuspto-grants-2013_10
ORD IDord-2a0aae788b74406e95e301771b969413
出典メモuspto-grants-2013_10