戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 356655作成日:2026年10月26日

4,6-Dichloro-5-(2-methoxy-phenoxy)-2-morpholin-4-yl-pyrimidine → 5-Isopropyl-pyridine-2-sulfonic acid 6-chloro-5-(2-methoxy-phenoxy)-2-morpholin-4-yl-pyrimidin-4-yl-amide

https://huagongshe.com/reaction/356655

反応式

関与物質

役割名称HCID仕込み量
反応物4,6-Dichloro-5-(2-methoxy-phenoxy)-2-morpholin-4-yl-pyrimidineHCID 21979531—
反応物5-Isopropyl pyridine-2-sulfonamide potassium saltHCID 131720944—
溶媒Dimethyl SulfoxideHCID 679—
生成物5-Isopropyl-pyridine-2-sulfonic acid 6-chloro-5-(2-methoxy-phenoxy)-2-morpholin-4-yl-pyrimidin-4-yl-amideHCID 2272940696.4%

反応手順

A solution of 1.18 g of 4,6-dichloro-5-(2-methoxy-phenoxy)-2-morpholin-4-yl-pyrimidine and 2.12 g (8.88 mmol) of 5-isopropyl-pyridine-2-sulphonamide potassium salt in 25 ml of dry DMSO was heated to 80° C. for 3 hours until the dichloride had disappeared completely. The DMSO was removed in a high vacuum, the residue was taken up with 60 ml of water and the aqueous solution was washed three times with diethyl ether. The solution was then acidified to pH 3.5 with 1N HCl and the product was extracted three times with ethyl acetate. The organic phases were washed twice with water and finally once with saturated sodium chloride solution, combined, dried with sodium sulphate and evaporated. The crystalline residue was digested twice with absolute diethyl ether in order to completely remove a trace of 5-isopropyl-pyridine-2-sulphonamide. The crystals remaining behind were filtered off and dried. There were obtained 1.66 g (96%) of 5-isopropyl-pyridine-2-sulphonic acid 6-chloro-5-(2-methoxy-phenoxy)-2-morpholin-4-yl-pyrimidin-4-ylamide as white crystals of m.p. 168°-176° C., MS: (M-H)- =518.3.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05837708
出典データセットuspto-grants-1998_11
ORD IDord-587d000b43c7457b8e3652f38cd3d8fa
出典メモuspto-grants-1998_11