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HRID 14558作成日:2026年10月25日

1,2,3,6-Tetrahydropyridine → 1-(6-(2-Butynyloxy)-5-fluoropyrimidin-4-yl)-1,2,3,6-tetrahydropyridine

https://huagongshe.com/reaction/14558

反応式

関与物質

役割名称HCID仕込み量
反応物1,2,3,6-TetrahydropyridineHCID 12750—
反応物4-(2-Butynyloxy)-5-fluoro-6-chloropyrimidineHCID 22599717—
生成物1-(6-(2-Butynyloxy)-5-fluoropyrimidin-4-yl)-1,2,3,6-tetrahydropyridineHCID 59341148101.4%

反応手順

0.2 g of 4-(2-butynyloxy)-6-chloro-5-fluoropyrimidine and 0.25 g of 1,2,3,6-tetrahydropyridine were mixed and left for 3 hours at room temperature. The reaction mixture was subjected to silica gel column chromatography to obtain 0.25 g of 1-(6-(2-butynyloxy)-5-fluoropyrimidin-4-yl)-1,2,3,6-tetrahydropyridine (hereinafter, referred to as Compound (53)).

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-83ad6d2e8682477ebd923d867eee68c3
出典メモuspto-grants-2010_06