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HRID 242925作成日:2026年10月27日

Diisopropylethylamine → [(R)-2-Benzyloxy-1-(6-fluoro-1-phenyl-1H-benzoimidazol-2-yl)ethyl]-(7H-purin-6-yl)amine

https://huagongshe.com/reaction/242925

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物6-chloro-9-(tetrahydro-2H-pyran-2-yl)-9H-purineHCID 97740—
反応物(R)-2-Benzyloxy-1-(6-fluoro-1-phenyl-1H-benzoimidazol-2-yl)ethylamineHCID 68157494—
溶媒1-ButanolHCID 263—
生成物[(R)-2-Benzyloxy-1-(6-fluoro-1-phenyl-1H-benzoimidazol-2-yl)ethyl]-(7H-purin-6-yl)amineHCID 6815772764.3%

反応条件

温度90 °C

反応手順

A mixture of (R)-2-benzyloxy-1-(6-fluoro-1-phenyl-1H-benzoimidazol-2-yl)ethylamine (298 mg, 0.83 mmol), 6-chloro-9-(tetrahydropyran-2-yl)-9H-purine (200 mg, 0.83 mmol) and DIPEA (700 μL, 4.2 mmol) in n-butanol (5 mL) was heated at 90° C. in a sealed vial for 48 h. After cooling to RT, the volatiles were removed in vacuo and the resulting residue loaded onto an Isolute® SCX-2 cartridge then washed with MeOH followed by 2M NH3/MeOH. The product containing fractions were combined and concentrated in vacuo. The resulting residue was purified by column chromatography (Si—PCC, gradient 0-10% 2M NH3/MeOH in DCM) to afford the title compound as a colourless oil (256 mg, 64%). LCMS (Method B): RT 3.26 min [M+H]+ 480.2.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08653089B2
出典データセットuspto-grants-2014_02
ORD IDord-5fdbc1da9afb46c4968c794f45b70cce
出典メモuspto-grants-2014_02