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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1708894Generated: October 31, 2026

(6R,7R)-7-[[(2Z)-2-[5-[(2-methylpropan-2-yl)oxycarbonylamino]-1,2,4-thiadiazol-3-yl]-2-[2-[(2-methylpropan-2-yl)oxy]-2-oxoethoxy]iminoacetyl]amino]-8-oxo-3-(3-oxobutanoyloxymethyl)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid → (6R,7R)-7-[[(2Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(carboxymethoxyimino)acetyl]amino]-8-oxo-3-(3-oxobutanoyloxymethyl)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

https://huagongshe.com/reaction/1708894

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(6R,7R)-7-[[(2Z)-2-[5-[(2-methylpropan-2-yl)oxycarbonylamino]-1,2,4-thiadiazol-3-yl]-2-[2-[(2-methylpropan-2-yl)oxy]-2-oxoethoxy]iminoacetyl]amino]-8-oxo-3-(3-oxobutanoyloxymethyl)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acidHCID 88417246—
SolventTrifluoroacetic acidHCID 6422—
Product(6R,7R)-7-[[(2Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-(carboxymethoxyimino)acetyl]amino]-8-oxo-3-(3-oxobutanoyloxymethyl)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acidHCID 1557523995.2%

Reaction Steps

To 50 ml of trifluoroacetic acid is added 23 g of 7β-[2-(5-tert-butoxycarbonylamino-1,2,4-thiadiazol-3-yl)-2(Z)-(tert-butoxycarbonylmethoxyimino)acetamido]-3-(3-oxobutyryloxymethyl)-3-cephem-4-carboxylic acid with stirring under ice-cooling. After removing the cooling-bath, the mixture is stirred for 1.5 hours. To the residue is added 50 ml of ethyl acetate and the solvent is evaporated off under reduced pressure. Fifty milliliter of ethyl acetate is added to the residue. Trituration and filtration of the resulting precipitate give 17 g of the above-identified compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04946837
Source datasetuspto-grants-1990_08
ORD IDord-929a1037de7d4737badc5a3b97148bc5
Source noteuspto-grants-1990_08