戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 14522作成日:2026年10月24日

3,5-Dimethylpiperidine → 4-(3,5-Dimethylpiperidino)-5-fluoro-6-(2-pentynyloxy)pyrimidine

https://huagongshe.com/ja/reaction/14522

反応式

関与物質

役割名称HCID仕込み量
反応物3,5-DimethylpiperidineHCID 118259—
反応物4-Chloro-5-fluoro-6-(2-pentynyloxy)pyrimidineHCID 59341120—
生成物4-(3,5-Dimethylpiperidino)-5-fluoro-6-(2-pentynyloxy)pyrimidineHCID 5782468584.7%

反応手順

0.2 g of 4-chloro-5-fluoro-6-(2-pentynyloxy)pyrimidine and 0.32 g of 3,5-dimethylpiperidine (cis/trans=about 3/1) were mixed and left for 3 hours at room temperature. The reaction mixture was subjected to silica gel column chromatography to obtain 0.23 g of 4-(3,5-dimethylpiperidino)-5-fluoro-6-(2-pentynyloxy)pyrimidine (hereinafter, referred to as Compound (11)). Compound (11) had the cis/trans diastereomer originated two methyls on the piperidine ring. The ratio of the cis/trans diastereomer was about 3.8/1.

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-359178bc0bbb4b3da86334cd14e4f2bb
出典メモuspto-grants-2010_06