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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 866875Generated: October 30, 2026

HCID 131711165, compound → HCID 131711164, compound

https://huagongshe.com/reaction/866875

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 131711165HCID 131711165—
SolventTrifluoroacetic acidHCID 6422—
SolventAnisoleHCID 7519—
ProductHCID 131711164HCID 13171116462%

Reaction Steps

A solution of 3-[2-(N-tertiary butoxycarbonylglycyl)hydrazono]methyl-7-(2-thienylacetamido)-3-cephem-4-carboxylic acid (120 mg) in a mixture of anisole (0.6 ml) and trifluoroacetic acid (1.2 ml) is kept at 0° C for 1 hour. The reaction mixture is concentrated to remove trifluoroacetic acid, and the obtained residue is diluted with ether. The separated crystals are washed with ether and water and dried to give 3-(2-glycylhydrazono)methyl-7-(2-thienylacetamido)-3-cephem-4-carboxylic acid (60 mg). m.p. 204°-209° C (decomposition). Yield: 62%. IR: νmax Nujol 3260, 1767, 1660, 1600, 1585cm-1. UV: νmaxEtOH 235nm; 316nm (Saturated solution). NMR: δd 6-DMSO 3.58s2H, 3.9dd2H, 5.17d(4Hz)1H, 5.75dd(8;4Hz)1H, 6.80-7.47m3H, 8.20s1H, 9.13d(8Hz)1H.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04101658
Source datasetuspto-grants-1978_07
ORD IDord-78234cc7765e49dca0a9a34991a83187
Source noteuspto-grants-1978_07