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HRID 543540作成日:2026年10月26日

Ammonia → 7-Amino-3-(1-methyltetrazol-5-ylthiomethyl)-3-cephem-4-carboxylicacid

https://huagongshe.com/reaction/543540

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物DacthalHCID 2943—
反応物7-Amino-3-(3-carboxypropionyloxy)methyl-3-cephem-4-carboxylic acidHCID 70463736—
反応物HCID 178482017HCID 178482017—
溶媒AcetonitrileHCID 6342—
生成物7-Amino-3-(1-methyltetrazol-5-ylthiomethyl)-3-cephem-4-carboxylicacidHCID 1302081388%

反応手順

A 4.0 ml portion of acetonitrile was added to 0.826 g of 7-amino-3-(3-carboxypropionyloxy)methyl-3-cephem-4-carboxylic acid and 0.32 g of 5-mercapto-1-methyl-1H-tetrazole, and 3.71 g of DCPA was added through a dropping funnel to the mixture under cooling at -5° to 0° C., followed by rinsing the funnel with 0.5 ml of acetonitrile. The mixture was stirred at the same temperature and turned into a solution. Then, the reaction solution was stirred for 45 minutes at 14° to 15° C. to allow the reaction to proceed. The reaction solution was cooled with ice, and poured into ice-water, which was placed in a refrigerator overnight and adjusted to pH 4.0 with 25% aqueous ammonia. The precipitated powder was recovered by filtration, washed with water and acetone successively, and dried, thereby affording 0.722 g (88.0% of yield) of 7-amino-3-(1-methyl-1H-tetrazol-5-yl)thiomethyl-3-cephem-4-carboxylic acid. The IR and NMR values of the product were in accordance with those of the authentic sample.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04446318
出典データセットuspto-grants-1984_05
ORD IDord-38ad118902834c5099dd535d6bec4efd
出典メモuspto-grants-1984_05