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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 356655생성일: 2026년 10월 25일

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

반응식

참여 물질

역할이름HCID투입량
반응물4,6-Dichloro-5-(2-methoxy-phenoxy)-2-morpholin-4-yl-pyrimidineHCID 21979531—
반응물5-Isopropyl pyridine-2-sulfonamide potassium saltHCID 131720944—
용매Dimethyl SulfoxideHCID 679—
생성물5-Isopropyl-pyridine-2-sulfonic acid 6-chloro-5-(2-methoxy-phenoxy)-2-morpholin-4-yl-pyrimidin-4-yl-amideHCID 2272940696.4%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05837708
출처 데이터셋uspto-grants-1998_11
ORD IDord-587d000b43c7457b8e3652f38cd3d8fa
출처 메모uspto-grants-1998_11