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HRID 257184作成日:2026年10月25日

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/257184

反応式

関与物質

役割名称HCID仕込み量
反応物5-(4-[2-(N-Methyl-N-(2-benzoxazolyl)amino)ethoxy]benzylidene)-2,4-thiazolidinedioneHCID 54450184—
反応物HCID 178418361HCID 178418361—
触媒PalladiumHCID 23938—
溶媒1,4-DioxaneHCID 31275—
生成物5-(4-[2-(N-Methyl-N-(2-benzoxazolyl)amino)ethoxy] benzyl)-2,4-thiazolidinedione hemihydrateHCID 88043875—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05260445
出典データセットuspto-grants-1993_11
ORD IDord-f41f193375cc4e47b8c1ff4e6e707bbc
出典メモuspto-grants-1993_11