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HRID 875944作成日:2026年10月26日

3-Chloro-4-pyridineboronic acid → 5-(3-Chloro-pyridin-4-yl)-N4-(tetrahydro-pyran-4-yl)-pyrimidine-2,4-diamine

https://huagongshe.com/reaction/875944

反応式

関与物質

役割名称HCID仕込み量
反応物3-Chloro-4-pyridineboronic acidHCID 3861877—
反応物5-Bromo-N4-(tetrahydro-pyran-4-yl)-pyrimidine-2,4-diamineHCID 58299673—
触媒HCID 178418476HCID 178418476—
溶媒1,4-DioxaneHCID 31275—
生成物5-(3-Chloro-pyridin-4-yl)-N4-(tetrahydro-pyran-4-yl)-pyrimidine-2,4-diamineHCID 5830002198%

反応条件

温度130 °C

反応手順

A mixture of compound 33 (2.03 g, 7.43 mmol), 3-chloropyridin-4-ylboronic acid (3.51 g, 22.3 mmol), and Pd(PPh3)2Cl2 (0.522 g, 0.743 mmol) in dioxane (44 ml) in a pressure vessel was purged with N2 for 20 minutes and to this mixture was added aq. Na2CO3 (1 M, 22 mL) by syringe. The reaction was further purged with N2 for another 20 minutes and then heated to 130° C. for 12 hours. DCM was added to the reaction and the mixture was washed with water and brine. The organic layer was dried with sodium sulfate and concentrated to provide compound 34 (2.07 g, crude, 98%) which was used in the next reaction without further purification. LCMS-ESI (POS), M/Z, M+1: Found 306.1, Calculated 306.1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08980903B2
出典データセットuspto-grants-2015_03
ORD IDord-4ffe5995e4ef4227aa7e7f5e8e681efe
出典メモuspto-grants-2015_03