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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2400967생성일: 2026년 10월 25일

N-(2,4-dioxothiazolidin-3-yl)methanesulfonamide → N-[(5Z)-5-({1-[4-Chloro-2-(trifluoromethyl)benzyl]-3-iodo-1H-indazol-5-yl}methylidene)-2,4-dioxo-1,3-thiazolidin-3-yl]methanesulfonamide

https://huagongshe.com/reaction/2400967

반응식

참여 물질

역할이름HCID투입량
반응물N-(2,4-dioxothiazolidin-3-yl)methanesulfonamideHCID 86659694—
반응물1-[4-Chloro-2-(trifluoromethyl)benzyl]-3-iodo-1H-indazol-5-carbaldehydeHCID 86659698—
생성물N-[(5Z)-5-({1-[4-Chloro-2-(trifluoromethyl)benzyl]-3-iodo-1H-indazol-5-yl}methylidene)-2,4-dioxo-1,3-thiazolidin-3-yl]methanesulfonamideHCID 58530445—

반응 단계

N-[(5Z)-5-({1-[4-Chloro-2-(trifluoromethyl)benzyl]-3-iodo-1H-indazol-5-yl}methylidene)-2,4-dioxo-1,3-thiazolidin-3-yl]methanesulfonamide was prepared from N-(2,4-dioxothiazolidin-3-yl)methanesulfonamide (from Example 360) and 1-[4-chloro-2-(trifluoromethyl)benzyl]-3-iodo-1H-indazol-5-carbaldehyde following General Procedure F.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08796256B2
출처 데이터셋uspto-grants-2014_08
ORD IDord-2bee6e0e2a434082a519da250421ea14
출처 메모uspto-grants-2014_08