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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 483028Generated: October 30, 2026

Methanesulfonic Acid → 7beta-amino-3-[(1-acetamido-1H-tetrazol-5-yl)thiomethyl]-3-cephem-4-carboxylic acid

https://huagongshe.com/reaction/483028

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantAmmonium HydroxideHCID 14923—
Reactant7-Aminocephalosporanic acidHCID 441328—
ReactantHCID 178475130HCID 178475130—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product7beta-amino-3-[(1-acetamido-1H-tetrazol-5-yl)thiomethyl]-3-cephem-4-carboxylic acidHCID 7045352875.4%

Reaction Conditions

Temperature50 °C

Reaction Steps

Methanesulfonic acid (5.77 g, 60 mmol) was added dropwise to a solution of 7β-aminocephalosporanic acid (3.27 g, 12.0 mmol) and 1-acetamido-5-mercapto-1H-tetrazole (2.50 g, 15.7 mmol) in acetonitrile (15 ml). The mixture was stirred at room temperature for 30 minutes and at 50° C. for 4 hours. Water (20 ml) was added with cooling to the reaction mixture, which was then adjusted to pH 3.5 with 28% aqueous ammonium hydroxide. Precipitates formed were filtered, washed with water and acetone successively and dried to give pale brown powder of 7β-amino-3-[(1-acetamido-1H-tetrazol-5-yl)thiomethyl]-3-cephem-4-carboxylic acid (3.36 g, 75. 3%), mp~195° C. (decomposition).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04576938
Source datasetuspto-grants-1986_03
ORD IDord-11119a67e57b42ec8ac5c67b25957fae
Source noteuspto-grants-1986_03