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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 642171생성일: 2026년 10월 26일

Methyl 3-[4-(chlorosulfonyl)phenyl]propanoate → Tert-butyl 2-[4-({[4-(3-methoxy-3-oxopropyl)phenyl]sulfonyl}amino)benzoyl]hydrazinecarboxylate

https://huagongshe.com/reaction/642171

반응식

참여 물질

역할이름HCID투입량
반응물Methyl 3-[4-(chlorosulfonyl)phenyl]propanoateHCID 23158517—
반응물Tert-butyl 2-(4-aminobenzoyl)hydrazinecarboxylateHCID 68409588—
용매PyridineHCID 1049—
용매Diethyl EtherHCID 3283—
생성물Tert-butyl 2-[4-({[4-(3-methoxy-3-oxopropyl)phenyl]sulfonyl}amino)benzoyl]hydrazinecarboxylateHCID 1029930156%

반응 단계

To a solution of tert-butyl 2-(4-aminobenzoyl)hydrazinecarboxylate (200 mg, 0.80 mmol) in anhydrous pyridine (4 mL) was added dropwise methyl 3-(4-chlorosulfonylphenyl)propionate (251 mg, 0.96 mmol) at rt. After 60 min, aminomethyl resin (Polymers Laboratories PL-AMS, 1.96 mmol/g, 200 mg) was added and the resulting mixture was stirred for 1 hr at rt. After filtration and rinsing the resin, water (100 mL) was added into the filtrate. Extraction with EtOAc (100 mL), washing with HCl (1N, 60 mL) and an aqueous saturated solution of NaHCO3 (50 mL), drying over MgSO4 and evaporation under vacuo gave a yellow oil. The residue was taken up in Et2O and a white solid precipitated out. Filtration and washing with Et2O gave the title compound (214 mg) was obtained as a white solid (56%) in 99.3% purity by HPLC (MaxPlot detection between 230 and 400 nm).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07696231B2
출처 데이터셋uspto-grants-2010_04
ORD IDord-ef6973d6faaa43b9a5fa8f786960a0d4
출처 메모uspto-grants-2010_04