돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1358366생성일: 2026년 10월 23일

4-Toluenesulfonyl chloride → 5-Methyl-pyridine-2-sulfonic acid {5-(2-methoxy-phenoxy)-2-pyridin-4-yl-6-[2-(toluene-4-sulfonylamino)-ethoxy]-pyrimidin-4-yl}-amide

https://huagongshe.com/ko/reaction/1358366

반응식

참여 물질

역할이름HCID투입량
반응물4-Toluenesulfonyl chlorideHCID 7397—
반응물5-methyl-N-[6-(2-aminoethoxy)-5-(o-methoxyphenoxy)-2-(4-pyridyl)-4-pyrimidinyl]-2-pyridine sulfonamideHCID 18184254—
생성물5-Methyl-pyridine-2-sulfonic acid {5-(2-methoxy-phenoxy)-2-pyridin-4-yl-6-[2-(toluene-4-sulfonylamino)-ethoxy]-pyrimidin-4-yl}-amideHCID 18184249—

반응 단계

According to the procedure described in Example 4a) 107 mg 5-methyl-N-[6-(2-aminoethoxy)-5-(o-methoxyphenoxy)-2-(4-pyridyl)-4-pyrimidinyl]-2-pyridine sulfonamide was reacted with 4-methylbenzenesulfonylchloride to give 70 mg 5-methyl-N-[6-(2-(4-methylbenzenesulfonylamino)-ethoxy)-5-(o-methoxyphenoxy)-2-(4-pyridyl)-4-pyrimidinyl]-2-pyridine sulfonamide. LC-MS: tR=4.55 min [M+1]+663.56, [M−1]−=661.63.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06596719B1
출처 데이터셋uspto-grants-2003_07
ORD IDord-67ab6b64667a49db9c38b8a421e6e3e1
출처 메모uspto-grants-2003_07