戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 37095作成日:2026年10月25日

Phosphorus pentachloride → 4-tert-butyl-N-[5-(2-chloro-5-methoxy-phenoxy)-6-chloromethyl-2-(morpholin-4-yl)-pyrimidin-4-yl]-benzenesulphonamide

https://huagongshe.com/reaction/37095

反応式

関与物質

役割名称HCID仕込み量
反応物Phosphorus pentachlorideHCID 24819—
反応物4-tert-butyl-N-[5-(2-chloro-5-methoxy-phenoxy)-6-hydroxymethyl-2-(morpholin-4-yl)-pyrimidin-4-yl]-benzenesulphonamideHCID 19934757—
溶媒Phosphorus oxychlorideHCID 24813—
生成物4-tert-butyl-N-[5-(2-chloro-5-methoxy-phenoxy)-6-chloromethyl-2-(morpholin-4-yl)-pyrimidin-4-yl]-benzenesulphonamideHCID 1993475563.8%

反応手順

4.57 g of 4-tert-butyl-N-[5-(2-chloro-5-methoxy-phenoxy)-6-hydroxymethyl-2-(morpholin-4-yl)-pyrimidin-4-yl]benzenesulphonamide in 50 ml of POCl3 were stirred with 2.03 g of PCl5 at 20° C. for 2 hours. Thereafter, the POCl3 was distilled off and the residue was partitioned between ethyl acetate and aqueous 1N NaOH. The organic phase was washed with water, dried and the solvent was evaporated. The residue was chromatographed over silica gel with dichloromethane and chloroform, thereafter recrystallized from dichloromethane-ethanol. There were obtained 3.01 g of 4-tert-butyl-N-[5-(2-chloro-5-methoxy-phenoxy)-6-chloromethyl-2-(morpholin-4-yl)-pyrimidin-4-yl]-benzenesulphonamide, m.p. 170° C., MS: M=581.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05420129
出典データセットuspto-grants-1995_05
ORD IDord-fc184ab77cc448dcb117f42007e8a033
出典メモuspto-grants-1995_05