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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 10947생성일: 2026년 10월 24일

Ethyl 3-{[(3'-{[(2-aminoanilino)carbothioyl]amino}[1,1'-biphenyl]-3-yl)sulfonyl]amino}-3-phenyl-propanoate → Ethyl 3-{[3'-(1H-benzimidazol-2-ylamino)[1,1'-biphenyl]3-yl]-sulfonylamino}-3-phenyl-propanoate

https://huagongshe.com/ko/reaction/10947

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl 3-{[(3'-{[(2-aminoanilino)carbothioyl]amino}[1,1'-biphenyl]-3-yl)sulfonyl]amino}-3-phenyl-propanoateHCID 21982385—
촉매Mercuric oxideHCID 30856—
용매ChloroformHCID 6212—
생성물Ethyl 3-{[3'-(1H-benzimidazol-2-ylamino)[1,1'-biphenyl]3-yl]-sulfonylamino}-3-phenyl-propanoateHCID 21982519—

반응 단계

43 g (75 mmol) of Ethyl 3-{[(3′-{[(2-aminoanilino)carbothioyl]amino}[1,1′-biphenyl]-3-yl)sulfonyl]amino}-3-phenyl-propanoate 11.1.1 and 16.24 g (75 mmol) of yellow mercury oxide were mixed with 1.51 CHCl3 and refluxed for 6 h. The resulting material was purified via flash chromatography (dichloromethane/acetic acid ethyl ester 3+1). Recrystallization from acetic acid ethyl ester led to 27.8 g (68%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07094911B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-660d63e58a12491cb152bc9a8923af2b
출처 메모uspto-grants-2006_08