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HRID 872297作成日:2026年10月25日

4-Methoxy-2-pyrimidinamine → tert-butyl N-[1-[4-(7-oxo-3-phenyl-1H-imidazo[1,2-a]pyrimidin-2-yl)phenyl]cyclobutyl]carbamate

https://huagongshe.com/reaction/872297

反応式

関与物質

役割名称HCID仕込み量
反応物4-Methoxy-2-pyrimidinamineHCID 67428—
反応物tert-Butyl (1-{4-[bromo(phenyl)acetyl]phenyl}cyclobutyl)carbamateHCID 86691038—
溶媒DimethylformamideHCID 6228—
生成物tert-butyl N-[1-[4-(7-oxo-3-phenyl-1H-imidazo[1,2-a]pyrimidin-2-yl)phenyl]cyclobutyl]carbamateHCID 178452600—

反応条件

温度90 °C

反応手順

A mixture of crude {1-[4-(2-bromo-2-phenyl-acetyl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl ester [Int-1-A] (1.26 g) and 4-methoxypyrimidin-2-ylamine (0.67 g) in DMF (21 mL) was heated overnight at 90° C. (bath temperature). On cooling the mixture was partitioned between EtOAc and water and the organic phase washed with brine, dried and concentrated to give a mixture of the title compound and Int-2-0. Purification was achieved by preparative HPLC to give the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08975265B2
出典データセットuspto-grants-2015_03
ORD IDord-f7044b18d69d4fd0b4a5a19715df59e5
出典メモuspto-grants-2015_03