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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2085090생성일: 2026년 10월 26일

4,6-Dichloro-5-(2-methoxyphenoxy)pyrimidine → 5-isopropyl-N-[6-chloro-5-(o-methoxyphenoxy)-4-pyrimidinyl]-2-pyridine sulfonamide

https://huagongshe.com/reaction/2085090

반응식

참여 물질

역할이름HCID투입량
반응물4,6-Dichloro-5-(2-methoxyphenoxy)pyrimidineHCID 15819130—
반응물5-Isopropyl pyridine-2-sulfonamide potassium saltHCID 131720944—
용매DimethylformamideHCID 6228—
생성물5-isopropyl-N-[6-chloro-5-(o-methoxyphenoxy)-4-pyrimidinyl]-2-pyridine sulfonamideHCID 2272940764.4%

반응 단계

A solution of 2.71 g of 4,6-dichloro-5-(o-methoxyphenoxy)-pyrimidine (Example 10b) and 5.0 g of 5-isopropyl pyridine-2-sulfonamide potassium salt (Example 1e) in 50 ml of DMF was stirred at room temperature for 20 h. The solvent was removed in vacuo, the residue was taken up in 200 ml of 10% aqueous acetic acid and extracted three times with ethyl acetate. The combined organic layers were washed with water and brine, dried over MgSO4 and evaporated. The crude product was crysallised from a mixture of 2-propanol and diethyl ether. The crystals were collected, washed with cold 2-propanol and diethyl ether and dried to give 2.8 g of 5-isopropyl-N-[6-chloro-5-(o-methoxyphenoxy)-4-pyrimidinyl]-2-pyridine sulfonamide as white crystals. LC-MS: tR=4.99 min, [M+1]+=435.25, [M−1]−=433.28.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06720322B2
출처 데이터셋uspto-grants-2004_04
ORD IDord-6dd33fb52f5a4519940194809d77d15b
출처 메모uspto-grants-2004_04