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HRID 14513作成日:2026年10月23日

2-Methylpiperidine → 4-(2-Butynyloxy)-5-fluoro-6-(2-methylpiperidino)pyrimidine

https://huagongshe.com/ja/reaction/14513

反応式

関与物質

役割名称HCID仕込み量
反応物2-MethylpiperidineHCID 7974—
反応物4-(2-Butynyloxy)-5-fluoro-6-chloropyrimidineHCID 22599717—
溶媒EthanolHCID 702—
生成物4-(2-Butynyloxy)-5-fluoro-6-(2-methylpiperidino)pyrimidineHCID 5934111571.1%

反応手順

Into 3 ml of ethanol was resolved 0.3 g of 4-(2-butynyloxy)-6-chloro-5-fluoropyrimidine, 0.45 g of 2-methylpyperidine was added therein, and the mixture was stirred for 5 hours under reflux condition. The reaction mixture was cooled to near room temperature and concentrated. The residue was subjected to silica gel column chromatography to obtain 0.28 g of 4-(2-butynyloxy)-5-fluoro-6-(2-methylpiperidino)pyrimidine (hereinafter, referred to as Compound (1)).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732448B2
出典データセットuspto-grants-2010_06
ORD IDord-128a683dc56a4a128028ba8b3f713edc
出典メモuspto-grants-2010_06