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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 263995생성일: 2026년 10월 25일

5-(4-[2-(N-Methyl-N-(2-benzoxazolyl)amino)ethoxy]benzylidene)-2,4-thiazolidinedione → 5-(4-[2-(N-Methyl-N-(2-benzoxazolyl)amino)ethoxy] benzyl)-2,4-thiazolidinedione hemihydrate

https://huagongshe.com/reaction/263995

반응식

참여 물질

역할이름HCID투입량
반응물5-(4-[2-(N-Methyl-N-(2-benzoxazolyl)amino)ethoxy]benzylidene)-2,4-thiazolidinedioneHCID 54450184—
반응물HCID 178418361HCID 178418361—
촉매PalladiumHCID 23938—
용매1,4-DioxaneHCID 31275—
생성물5-(4-[2-(N-Methyl-N-(2-benzoxazolyl)amino)ethoxy] benzyl)-2,4-thiazolidinedione hemihydrateHCID 88043875—

반응 단계

5-(4-[2-(N-Methyl-N-(2-benzoxazolyl)amino)ethoxy]benzylidene)-2,4-thiazolidinedione (1.5 g) in dry 1,4-dioxan (80 ml) was reduced under hydrogen in the presence of 10% palladium on charcoal (2 g) at ambient temperature and atmospheric pressure until hydrogen uptake ceased. The solution was filtered through diatomaceous earth, the filter pad was washed exhaustively with dioxan and the combined filtrates were evaporated to dryness under vacuum. The title compound (mp 147°-9° C.) was obtained after crystallisation from methanol.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05646169
출처 데이터셋uspto-grants-1997_07
ORD IDord-d7b30d1548f04ed79cbfa1fd229d4a50
출처 메모uspto-grants-1997_07