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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1082277생성일: 2026년 10월 26일

Hydrochloric Acid → N-(6-[2-{6-(4-tert-butylphenylsulfonylamino)-5-(4-methylphenyl)pyrimidin-4-yloxy}ethoxy]pyridin-3-yl)benzamide

https://huagongshe.com/reaction/1082277

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Benzoyl chlorideHCID 7412—
반응물N-{6-{2-(5-aminopyridin-2-yloxy)ethoxy}-5-(4-methylphenyl)pyrimidin-4-yl}-4-tert-butylbenzenesulfonamideHCID 19689480—
용매PyridineHCID 1049—
용매DichloromethaneHCID 6344—
생성물N-(6-[2-{6-(4-tert-butylphenylsulfonylamino)-5-(4-methylphenyl)pyrimidin-4-yloxy}ethoxy]pyridin-3-yl)benzamideHCID 1968953189.8%

반응 단계

To a solution of N-{6-{2-(5-aminopyridin-2-yloxy)ethoxy}-5-(4-methylphenyl)pyrimidin-4-yl}-4-tert-butylbenzenesulfonamide (150 mg) in pyridine (2 ml) is added a solution of benzoyl chloride (43 mg) in methylene chloride (0.4 ml), and the mixture is stirred at room temperature for two hours. To the reaction solution is added 10% hydrochloric acid, and the mixture is extracted with ethyl acetate. The ethyl acetate layer is washed, dried and evaporated to remove the solvent. The residue is recrystallized from ethyl acetate/n-hexane to give N-(6-[2-{6-(4-tert-butylphenylsulfonylamino)-5-(4-methylphenyl)pyrimidin-4-yloxy}ethoxy]pyridin-3-yl)benzamide (161 mg) as crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05589478
출처 데이터셋uspto-grants-1996_12
ORD IDord-ec32215489264d80929487267dafd32d
출처 메모uspto-grants-1996_12