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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 128882Generated: November 1, 2026

(4-methoxyphenyl)methyl (6R)-7-[[(2Z)-2-[(2S)-1-benzhydryloxy-1-oxopropan-2-yl]oxyimino-2-[2-(tritylamino)-1,3-thiazol-4-yl]acetyl]amino]-3-(chloromethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate → HCID 178491526, compound

https://huagongshe.com/reaction/128882

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-methoxyphenyl)methyl (6R)-7-[[(2Z)-2-[(2S)-1-benzhydryloxy-1-oxopropan-2-yl]oxyimino-2-[2-(tritylamino)-1,3-thiazol-4-yl]acetyl]amino]-3-(chloromethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylateHCID 88420502—
ReactantHCID 178480134HCID 178480134—
ProductHCID 178491526HCID 17849152688%

Reaction Steps

Using 306 mg of p-methoxybenzyl 7-[(Z)-2-(2-tritylaminothiazol-4-yl)-2-{(S)-1-diphenylmethoxycarbonylethoxyimino}acetamido]-3-chloromethyl-3-cephem-4-carboxylate and 153 mg of 1,5-dimethyl-2-mercaptoimidazolo[4,5-c]pyridinium trifluoroacetate in place of p-methoxybenzyl 7-{(Z)-2-(2-tritylaminothiazol-4-yl)-2-methoxyiminoacetamido}-3-chloromethyl-3-cephem-4-carboxylate and 2-mercapto-4-methylthiazolo[5,4-b]pyridinium trifluoroacetate, respectively, the reaction and purification were carried out in the same manner as in Example 15(a) to obtain 334 mg of the title compound in a yield of 88%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05464829
Source datasetuspto-grants-1995_11
ORD IDord-20c5c5b208fe4b55a1ae70b04fed64ce
Source noteuspto-grants-1995_11