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HRID 508653作成日:2026年10月23日

2-Chloro-5-nitropyrimidine → HCID 53260086、化合物

https://huagongshe.com/ja/reaction/508653

反応式

関与物質

役割名称HCID仕込み量
反応物2-Chloro-5-nitropyrimidineHCID 82544—
反応物Sodium BicarbonateHCID 516892—
反応物HCID 12134904HCID 12134904—
触媒HCID 178418397HCID 178418397—
溶媒TolueneHCID 1140—
生成物HCID 53260086HCID 5326008619%

反応条件

温度90 °C

反応手順

To a solution of 3-(1-adamantyl)-4-benzyloxyphenylboronic acid (1) (833 g, 2.3 mmol) and 2-chloro-5-nitropyrimidine (2) (320 mg, 2.00 mmol) in degassed toluene (15 mL) was added tetrakis(triphenylphosphine)palladium (347 mg, 0.300 mmol), NaHCO3 (336 mg, 4.00 mmol) and degassed H2O (3 mL). The mixture was heated at reflux (90° C. oil-bath) for 24 h, cooled to room temperature and extracted with EtOAc (180 mL). The extract was washed (H2O and brine) and dried. After solvent removal at reduced pressure, the residue was chromatographed (3% EtOAc/hexane) to give 165 mg (19%) of 2-[3-(1-adamantyl)-4-benzyloxyphenyl]-5-nitropyrimidine as a yellow solid, mp 206° C. (dec). IR 2902, 1405, 1179 cm−1; 1H NMR (CDCl3) δ 1.76 (bs, 6H, AdCH2), 2.09 (bs, 311, AdCH), 2.22 (m, 6H, AdCH2), 5.24 (s, 2H, C6H5CH2), 7.07 (d, J=8.7 Hz, 1H, 5′-ArH), 7.34-7.53 (m, 5H, C6H5), 8.40 (dd, J=8.7 Hz, 2.4 Hz, 1H, 6′-ArH), 8.51 (d, J=2.4 Hz, 1H, 2′-ArH), 9.46 ppm (s, 2H, 4-ArH, 6-ArH). HRMS calcd C27H27N3O3 [M+H]+ 442.2125. found 442.2137.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09096544B2
出典データセットuspto-grants-2015_08
ORD IDord-ff0bd70eb6a4423f90afdcec38042ca9
出典メモuspto-grants-2015_08