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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2085082생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/2085082

반응식

참여 물질

역할이름HCID투입량
반응물4,6-Dichloro-5-(o-methoxyphenoxy)-2-methyl-pyrimidineHCID 21979599—
반응물5-Isopropyl pyridine-2-sulfonamide potassium saltHCID 131720944—
용매Dimethyl SulfoxideHCID 679—
용매WaterHCID 962—
생성물5-isopropyl-N-[6-chloro-5-(o-methoxyphenoxy)-2-methyl-4-pyrimidinyl]-2-pyridine sulfonamideHCID 2272940193.1%

반응 단계

To a solution of 2.15 g of 4,6-dichloro-5-(o-methoxyphenoxy)-2-methyl-pyrimidine in 40 ml of DMSO was added 3.59 g of 5-isopropyl-2-pyridine sulfonamide potassium salt. The mixture was stirred for 72 h at room temperature. The solution was diluted with 350 ml of water and extracted twice with 200 ml of diehtyl ether. The organic layers were extracted twice with water. The combined aqueous layers were acidified to pH 4 with 5 ml of acetic acid and extracted twice with DCM. The organic layers were washed with water, and dried over Na2SO4. The solution was treated with activated charcoal, filtered over Celite and evaporated. The residue was suspended in 30 ml of diethyl ether, filtered off and dried to give 3.15 g of 5-isopropyl-N-[6-chloro-5-(o-methoxyphenoxy)-2-methyl-4-pyrimidinyl]-2-pyridine sulfonamide as a pale beige powder. LC-MS: tR=5.18 min, [M+1]+=449.25, [M−1]−=447.31.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06720322B2
출처 데이터셋uspto-grants-2004_04
ORD IDord-33b8d669455141b1b145455a0e5b113b
출처 메모uspto-grants-2004_04