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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1654560Generated: October 31, 2026

Triethylamine → (4-methoxyphenyl)methyl (6R)-7-[[(2Z)-2-[(1R)-2-benzhydryloxy-1-(3,4-dihydroxyphenyl)-2-oxoethoxy]imino-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

https://huagongshe.com/reaction/1654560

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPhosphorus oxychlorideHCID 24813—
Reactant4-Methoxybenzyl 7-amino-3-chloromethyl-3-cephem-4-carboxylateHCID 14032022—
Reactant(2Z)-2-[(1R)-2-benzhydryloxy-1-(3,4-dihydroxyphenyl)-2-oxoethoxy]imino-2-[2-(tritylamino)-1,3-thiazol-4-yl]acetic acidHCID 15780328—
Product(4-methoxyphenyl)methyl (6R)-7-[[(2Z)-2-[(1R)-2-benzhydryloxy-1-(3,4-dihydroxyphenyl)-2-oxoethoxy]imino-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 16183830100.7%

Reaction Steps

By using 4.57 g (6 mmol) of (Z)-2-[[(R)-α-benzhydryloxycarbonyl-3,4-dihydroxybenzyl]oxyimino]-2-(2-tritylaminothiazol-4-yl)acetic acid, 2.03 g (5 mmol) of p-methoxybenzyl 7-amino-3-chloromethyl-3-cephem-4-carboxylate, 1.39 ml (10 mmol) and 0.84 ml (6 mmol) of triethylamine and 0.75 ml (8 mmol) of phosphorus oxychloride, the treatment was conducted in the same manner as in Example 1 (A) to obtain 5.60 g (yield: 56%) of p-methoxybenzyl 7-[(Z)-2-[[(R)-α-benzhydryloxycarbonyl-3,4-dihydroxybenzyl]oxyimino]-2-(tritylaminothiazol-4-yl)acetamido]-3-chloromethyl-3-cephem-4-carboxylate as a foam-like solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05407930
Source datasetuspto-grants-1995_04
ORD IDord-6d2a507f3f194e5d81765677f42080cb
Source noteuspto-grants-1995_04