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HRID 43071作成日:2026年10月24日

1-Isopropylpiperazine → 2-(4-Isopropyl-piperazin-1-yl)-5-nitro-pyrimidine

https://huagongshe.com/ja/reaction/43071

反応式

関与物質

役割名称HCID仕込み量
反応物1-IsopropylpiperazineHCID 78013—
反応物2-Chloro-5-nitropyrimidineHCID 82544—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物2-(4-Isopropyl-piperazin-1-yl)-5-nitro-pyrimidineHCID 6691466789.1%

反応条件

温度5 °C

反応手順

1-Isopropyl-piperazine (1.8 mL, 12.7 mmol, 2 equiv) was added to a cold (5° C.) solution of 2-chloro-5-nitropyrimidine (1 g, 6.3 mmol,) in DCM (5 mL). The reaction mixture was stirred for 20 min at 5° C. and then diluted with DCM and H2O. The aqueous layer was separated and extracted with DCM. The organic phase was washed with brine, dried (Na2SO4), filtered and concentrated to provide 1.41 g of the title compound as a beige solid: ESI-MS: 252.2 [M+H]+; tR=1.89 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08536175B2
出典データセットuspto-grants-2013_09
ORD IDord-9d3642df068f43569df35b2a9c34155a
出典メモuspto-grants-2013_09