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HRID 261313作成日:2026年10月25日

N-chloro-N-methyl-p-toluenesulfonamide → p-Nitrobenzyl 3-Methyl-2-(2-chlorosulfinyl-4-oxo-3-phenoxyacetamido-1-azetidinyl)-3-butenoate

https://huagongshe.com/reaction/261313

反応式

関与物質

役割名称HCID仕込み量
反応物N-chloro-N-methyl-p-toluenesulfonamideHCID 13017215—
反応物p-Nitrobenzyl 6-phenoxyacetamido-2,2-dimethylpenam-3-carboxylate-1-oxideHCID 67928276—
生成物p-Nitrobenzyl 3-Methyl-2-(2-chlorosulfinyl-4-oxo-3-phenoxyacetamido-1-azetidinyl)-3-butenoateHCID 9936995—

反応手順

To 150 ml. of distilled and molecular sieve-dried toluene were added 3.0 g. (6 mmol.) of p-nitrobenzyl 6-phenoxyacetamido-2,2-dimethylpenam-3-carboxylate-1-oxide and 1.3 g. (6 mmol.) of N-chloro-N-methyl-p-toluenesulfonamide. The mixture was heated at reflux for 60 minutes. The resulting reaction mixture then was cooled to room temperature. An aliquot (15 ml.) was separated, washed with water, and brine, dried over magnesium sulfate, and evaporated to dryness in vacuo. The nmr spectrum of the residue was consistent for the title compound contaminated with some N-methyl-p-toluenesulfonamide.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04165315
出典データセットuspto-grants-1979_08
ORD IDord-a641228144254f99a5c289426dabe60c
出典メモuspto-grants-1979_08