돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 38139생성일: 2026년 10월 25일

Oxalyl chloride → N-[(5-chloro(2-thienyl))sulfonyl]-N'-[4-(5-chloro-1,3-dioxobenzo [c]azolidin-2-yl)-3-methylphenyl]ethane-1,2-diamide

https://huagongshe.com/reaction/38139

반응식

참여 물질

역할이름HCID투입량
반응물Oxalyl chlorideHCID 65578—
반응물N-(4-Amino-o-tolyl)-4-chlorophthalimideHCID 93991—
반응물5-Chlorothiophene-2-SulfonamideHCID 1241301—
생성물N-[(5-chloro(2-thienyl))sulfonyl]-N'-[4-(5-chloro-1,3-dioxobenzo [c]azolidin-2-yl)-3-methylphenyl]ethane-1,2-diamideHCID 2080025744%

반응 단계

A 200 mg (1.0 mmol) of 5-chlorothiophenesulfonamide was slurried in 0.5 mL of oxalyl chloride and refluxed for 6 h. The solvent was removed in vacuo and 36 mg of the resulting solid was dissolved in 240 μL acetonitrile and treated with 40 mg (0.14 mmol) 2-(4-amino-2-methylphenyl)-5-chlorobenzo[c]azoline-1,3-dione. After stirring for 1 h, the solvent was removed and the residue was purified by RP-HPLC to give 33 mg (44%) of the titled compound. ES-MS (M+H)+=538(2Cl).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524721B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-9ec4754677b44b32a431031ad2edb79d
출처 메모uspto-grants-2013_09