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HRID 2082024作成日:2026年10月25日

Water → Benzhydryl 7beta-tert-butoxycarbonylamino-3-[3-formamido-2-(2-formyloxyethyl)-1-pyrazolio]methyl-3-cephem-4-carboxylate iodide

https://huagongshe.com/reaction/2082024

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sodium IodideHCID 5238—
反応物2-(5-Formamido-1H-pyrazol-1-yl)ethyl formateHCID 14996567—
反応物Benzhydryl 7beta-tert-butoxycarbonyl-amino-3-chloromethyl-3-cephem-4-carboxylateHCID 131717748—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物Benzhydryl 7beta-tert-butoxycarbonylamino-3-[3-formamido-2-(2-formyloxyethyl)-1-pyrazolio]methyl-3-cephem-4-carboxylate iodideHCID 10259694—

反応手順

To a mixture of benzhydryl 7β-tert-butoxycarbonyl-amino-3-chloromethyl-3-cephem-4-carboxylate (20 g) and sodium iodide (5.82 g) in N,N-dimethylformamide (20 ml) was added 5-formamido-1-(2-formyloxyethyl)pyrazole (21.34 g) at room temperature. After being stirred for 24 hours at the same temperature, the mixture was poured into a mixture of water and ethyl acetate. The organic layer was separated and washed with water, aqueous sodium chloride solution, and dried over magnesium sulfate. The solution was evaporated in vacuo to give benzhydryl 7β-tert-butoxycarbonylamino-3-[3-formamido-2-(2-formyloxyethyl)-1-pyrazolio]methyl-3-cephem-4-carboxylate iodide (29.6 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05187160
出典データセットuspto-grants-1993_02
ORD IDord-76cf50f6956a4814b12c62e399c37a74
出典メモuspto-grants-1993_02