戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1409740作成日:2026年10月25日

1,4-Dioxa-8-azaspiro(4.5)decane → 8-(5-Chloropyrimidin-2-yl)-1,4-dioxa-8-azaspiro[4.5]decane

https://huagongshe.com/reaction/1409740

反応式

関与物質

役割名称HCID仕込み量
反応物1,4-Dioxa-8-azaspiro(4.5)decaneHCID 67435—
反応物2,5-DichloropyrimidineHCID 590641—
溶媒DimethylformamideHCID 6228—
溶媒TriethylamineHCID 8471—
溶媒1,4-DioxaneHCID 31275—
生成物8-(5-Chloropyrimidin-2-yl)-1,4-dioxa-8-azaspiro[4.5]decaneHCID 68290179—

反応条件

温度120 °C

反応手順

1,4-Dioxa-8-azaspiro[4.5]decane (2.39 g) is combined with 2,5-dichloropyrimidine (2.44 g) in N,N-dimethylformamide (50 mL), 1,4-dioxane (75 mL) and triethylamine (6.7 mL) in a glass pressure reaction vessel and heated with stirring at 120° C. for 16 h. After cooling the orange solution is concentrated and partitioned between dichloromethane (100 mL) and water (100 mL). The water layer is extracted with dichloromethane (100 mL). The dichloromethane layers are combined, washed with water (2×100 mL), dried over Na2SO4, filtered and concentrated to give the title compound. LC (method 20): tR=2.24 min; Mass spectrum (APCI): m/z=256 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08921398B2
出典データセットuspto-grants-2014_12
ORD IDord-9492327c6cc84f15a0783ecd35ed93a1
出典メモuspto-grants-2014_12