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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1358348생성일: 2026년 10월 26일

4,6-Dichloro-5-(o-methoxyphenoxy)-2-methyl-pyrimidine → p-tert-butyl-N-[6-chloro-5-(o-methoxyphenoxy)-2-methyl-4-pyrimidinyl]benzenesulfonamide

https://huagongshe.com/reaction/1358348

반응식

참여 물질

역할이름HCID투입량
반응물4,6-Dichloro-5-(o-methoxyphenoxy)-2-methyl-pyrimidineHCID 21979599—
반응물HCID 131721323HCID 131721323—
용매Dimethyl SulfoxideHCID 679—
용매WaterHCID 962—
생성물p-tert-butyl-N-[6-chloro-5-(o-methoxyphenoxy)-2-methyl-4-pyrimidinyl]benzenesulfonamideHCID 1818422364.8%

반응 단계

To a solution of 1.0 g of 4,6-dichloro-5-(o-methoxyphenoxy)-2-methyl-pyrimidine in 20 ml of DMSO was added 1.76 g of 4-tert.-butyl-benzene sulfonamide potassium salt. The mixture was stirred for 72 h at room temperature. The solution was diluted with 250 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 cooled to 0° C. The precipitated product was filtered off and dried in vacuo to give 1.05 g of 4-tert.-butyl-N-[6-chloro-5-(o-methoxyphenoxy)-2-methyl-4-pyrimidinyl]-benzene sulfonamide as a pale beige powder. LC-MS: tR=5.64 min, [M+1]+=462.51, [M−1]−=460.63.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06596719B1
출처 데이터셋uspto-grants-2003_07
ORD IDord-c067f942e3544ed5b777df1160b0b3a0
출처 메모uspto-grants-2003_07