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HRID 26039作成日:2026年10月23日

N,N-Diethylaniline → Benzhydryl 7-cyanomethylthioacetamido-3-(1-methyl-1H-tetrazol-5-yl)vinyl-3-cephem-4-carboxylate

https://huagongshe.com/ja/reaction/26039

反応式

関与物質

役割名称HCID仕込み量
反応物N,N-DiethylanilineHCID 7061—
反応物Cyanomethylthioacetyl chlorideHCID 19989189—
反応物benzhydryl 7-amino-3-(1-methyl-1H-tetrazol-5-yl)vinyl-3-cephem-4-carboxylateHCID 131711470—
溶媒TetrahydrofuranHCID 8028—
生成物Benzhydryl 7-cyanomethylthioacetamido-3-(1-methyl-1H-tetrazol-5-yl)vinyl-3-cephem-4-carboxylateHCID 131711469—

反応手順

To 244 mg of benzhydryl 7-amino-3-(1-methyl-1H-tetrazol-5-yl)vinyl-3-cephem-4-carboxylate in 20 ml of anhydrous tetrahydrofuran were added dropwise at -7° C. with stirring 115 mg of N,N-diethylaniline and, subsequently, 115 mg of cyanomethylthioacetyl chloride in 5 ml of anhydrous tetrahydrofuran. After completion of the reaction, the reaction mixture was then treated in the same manner as in Example 1--(a) to give a crude product. The crude product was purified by developing it with ethyl acetate by the use of silica gel thin layer chromatography (20×20×0.2 cm) to yield 50 mg of benzhydryl 7-cyanomethylthioacetamido-3-(1-methyl-1H-tetrazol-5-yl)vinyl-3-cephem-4-carboxylate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04147863
出典データセットuspto-grants-1979_04
ORD IDord-9ccf351a7ed6494b8dcd9d01fb533e95
出典メモuspto-grants-1979_04