戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 251449作成日:2026年10月25日

Potassium Carbonate → 2-(6-Chloropyridin-3-yl)-3-oxa-1-azaspiro[4.5]dec-1-ene

https://huagongshe.com/reaction/251449

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物Thionyl ChlorideHCID 24386—
反応物6-chloro-N-[1-(hydroxymethyl)cyclohexyl]nicotinamideHCID 11950360—
溶媒ChloroformHCID 6212—
生成物2-(6-Chloropyridin-3-yl)-3-oxa-1-azaspiro[4.5]dec-1-eneHCID 1195072155%

反応手順

To a solution of 6-chloro-N-[1-(hydroxymethyl)cyclohexyl]nicotinamide ax47 (2.17 g, 8.06 mmol, 1 eq) in chloroform (80 ml) is added thionyl chloride (1.8 ml, 24.18 mmol, 3 eq). The mixture is stirred at reflux for 2 h 30 before removing the volatiles under vacuum. The residue is dissolved in acetone and treated with potassium carbonate (2 eq), at reflux. After an aqueous work-up, the organic phase is dried over magnesium sulfate and concentrated in vacuo to give 1.86 g of a yellow solid. Purification over silicagel (eluent: dichloromethane/methanol/ammonia 99:1:0.1) finally yields 0.56 g of 2-(6-chloropyridin-3-yl)-3-oxa-1-azaspiro[4.5]dec-1-ene ax49.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07863450B2
出典データセットuspto-grants-2011_01
ORD IDord-f7e4fe3ff9b64a1485d62ca2f11d7cf4
出典メモuspto-grants-2011_01