돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2085083생성일: 2026년 10월 24일

Water → 5-methyl-N-[6-chloro-5-(o-methoxyphenoxy)-2-methyl-4-pyrimidinyl]-2-pyridine sulfonamide

https://huagongshe.com/ko/reaction/2085083

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물4,6-Dichloro-5-(o-methoxyphenoxy)-2-methyl-pyrimidineHCID 21979599—
반응물5-Methyl-2-pyridine sulfonamide potassium saltHCID 131723992—
용매Dimethyl SulfoxideHCID 679—
생성물5-methyl-N-[6-chloro-5-(o-methoxyphenoxy)-2-methyl-4-pyrimidinyl]-2-pyridine sulfonamideHCID 2272939776.6%

반응 단계

At room temperature 2.95 g of 5-methyl-2-pyridine sulfonamide potassium salt (Example 3c) was added to a suspension of 2 g of 4,6-dichloro-5-(o-methoxyphenoxy)-2-methyl-pyrimidine (Example 7b) in 30 ml DMSO. The mixture was stirred at room temperature for 48 h and was then poured onto 300 ml of water. The aqueous solution was extracted twice with 200 ml of diethyl ether. The organic layers were extracted with water and the aqueous layers were combined and acidified with 3 ml of acetic acid to pH 4. Precipitation of the product was enhanced by adding 100 ml of saturated aqueous sodium chloride and cooling the mixture to 0° C. Eventually, the precipitate was filtered off, washed with cold water and dried under high vacuum to give 2.26 g of 5-methyl-N-[6-chloro-5-(o-methoxyphenoxy)-2-methyl-4-pyrimidinyl]-2-pyridine sulfonamide as a beige powder. LC-MS: tR=4.79 min, [M+1]+=421.42, [M−1]−=419.46.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06720322B2
출처 데이터셋uspto-grants-2004_04
ORD IDord-e4804a749a5c4e4f8d12564af1fd547c
출처 메모uspto-grants-2004_04