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HRID 260540作成日:2026年10月26日

4-Pentenoyl chloride → N,N'-Bis[2-(acetyloxy)-1-[(acetyloxy)-methyl]ethyl]-2,4,6-triiodo-5-[(1-oxo-4-pentenyl) amino]-1,3-benzenedicarboxamide

https://huagongshe.com/reaction/260540

反応式

関与物質

役割名称HCID仕込み量
反応物4-Pentenoyl chlorideHCID 4228493—
反応物N,N'-Bis[2-(acetyloxy)-1-[(acetyloxy)methyl]ethyl]-5-amino-2,4,6-triiodo-1,3-benzenedicarboxamideHCID 11766168—
溶媒DimethylacetamideHCID 31374—
生成物N,N'-Bis[2-(acetyloxy)-1-[(acetyloxy)-methyl]ethyl]-2,4,6-triiodo-5-[(1-oxo-4-pentenyl) amino]-1,3-benzenedicarboxamideHCID 1037369189%

反応手順

4-Pentenoyl chloride (11.9 g, 100 mmol) was added to a stirred solution of N,N'-bis-[2-(acetyloxy)-1-[(acetyloxy)-methyl]ethyl]-5-amino-2,4,6 -triiodo-1,3-benzenedicarboxamide (47.75 g, 50 mmol) in dimethylacetamide (400 mL) at room temperature and the mixture was stirred for 16 hours. Dimethylacetamide was removed in vacuo and the residue dissolved in ethyl acetate (600 ml). The solution was washed with aqueous sodium bicarbonate (10%, 2×150 mL) and with water (2×100 mL) and brine (150 mL). The organic layer was dried and the solvent removed to obtain the crude product as an off-white solid. Further purification by crystallization from a mixture of acetone (250 mL) and hexane (75 mL) afforded the title A compound (42.5 g), m.p. 162°-64°. TLC: Rf 0.55 in ethyl acetate. Mass Spectrum: m/z 956 (M+H)+, 830, 653.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05527926
出典データセットuspto-grants-1996_06
ORD IDord-a227adb5584347019e9cf0455f838307
出典メモuspto-grants-1996_06