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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 904873Generated: October 30, 2026

Ammonia → 7-amino 3-[1-(2-carboxy-2-methoxyiminoethyl)-1H-tetrazol-5-yl]thiomethyl-3-cephem-4-carboxylic acid

https://huagongshe.com/reaction/904873

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantBoron trifluoride etherateHCID 8000—
Reactant7-Aminocephalosporanic acidHCID 441328—
ReactantHCID 178502658HCID 178502658—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product7-amino 3-[1-(2-carboxy-2-methoxyiminoethyl)-1H-tetrazol-5-yl]thiomethyl-3-cephem-4-carboxylic acidHCID 13171324364%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a suspension of 7-aminocephalosporanic acid (0.99 g) and 1-(2-carboxy-2-methoxyiminoethyl)-1H-tetrazole-5-thiol (0.95 g) in dry acetonitrile (10 ml) was added boron trifluoride etherate (1.55 g) and the resulting solution was stirred at 50° C. for 2 hours. Water (10 ml) was added to the reaction mixture and the solution was adjusted to pH 3.5 with conc. aqueous ammonia under ice-cooling to give precipitates which were filtered, washed with water and dried to give 7-amino-3-[1-(2-carboxy-2-methoxyiminoethyl)-1H-tetrazol-5-yl)thiomethyl-3-cephem-4-carboxylic acid (1.0 g), mp 170° to 180° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04420477
Source datasetuspto-grants-1983_12
ORD IDord-676f381d00794af2b5830e28e6d7c10c
Source noteuspto-grants-1983_12