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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 412370생성일: 2026년 10월 26일

Triethylamine → N-[4-[2-[4-(2,4-Dioxothiazolidin-5-ylmethyl)phenoxymethyl]-1-methyl-1H-benzimidazol-6-yloxy]phenyl]naphthalene-2-carboxamide

https://huagongshe.com/reaction/412370

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2-Naphthoyl chlorideHCID 75246—
반응물5-[4-[6-(4-aminophenoxy)-1-methyl-1H-benzimidazol-2-ylmethoxy]benzyl]thiazolidine-2,4-dione dihydrochlorideHCID 86587768—
용매DimethylformamideHCID 6228—
생성물N-[4-[2-[4-(2,4-Dioxothiazolidin-5-ylmethyl)phenoxymethyl]-1-methyl-1H-benzimidazol-6-yloxy]phenyl]naphthalene-2-carboxamideHCID 1014590873.4%

반응 단계

A reaction was conducted by a similar procedure to that described in Example 52 using triethylamine (0.32 ml), 2-naphthoyl chloride (153 mg), 5-[4-[6-(4-aminophenoxy)-1-methyl-1H-benzimidazol-2-ylmethoxy]benzyl]thiazolidine-2,4-dione dihydrochloride (400 mg) and anhydrous N,N-dimethylformamide (8 ml). The reaction mixture was concentrated under reduced pressure. To the residue was added ethyl acetate and water. The precipitate was isolated by filtration to afford the title compound (337 mg, white powder, mp 221-223° C.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06562849B1
출처 데이터셋uspto-grants-2003_05
ORD IDord-30fc791967ed4708876ca7c2b0f5afde
출처 메모uspto-grants-2003_05