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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 894825Generated: October 25, 2026

Bromotrimethylsilane → (6R,7R)-7-[[(2Z)-2-(furan-2-yl)-2-methoxyiminoacetyl]amino]-8-oxo-3-(phosphonocarbamoyloxymethyl)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

https://huagongshe.com/reaction/894825

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromotrimethylsilaneHCID 76113—
ReactantN-trimethylsilylurethaneHCID 11355656—
Reactant(6R,7R)-3-(dimethoxyphosphorylcarbamoyloxymethyl)-7-[[(2Z)-2-(furan-2-yl)-2-methoxyiminoacetyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acidHCID 88764320—
SolventDichloromethaneHCID 6344—
Product(6R,7R)-7-[[(2Z)-2-(furan-2-yl)-2-methoxyiminoacetyl]amino]-8-oxo-3-(phosphonocarbamoyloxymethyl)-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acidHCID 88760882—

Reaction Steps

Bromotrimethylsilane (0.61 g), in dichloromethane (3 ml) was added (at 0° under nitrogen) to a stirred solution of (6R,7R)-3-dimethoxyphosphorylcarbamoyloxymethyl-7-[Z-2-(fur-2-yl)-2-methoxyiminoacetamido]ceph-3-em-4-carboxylic acid (0.53 g) and trimethylsilylurethane (0.965 g) in dry dichloromethane (5 ml). After 1.75 hours no starting cephalosporin remained as indicated by t.l.c.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04284766
Source datasetuspto-grants-1981_08
ORD IDord-1ba7a33139484ec0a62fe7bfe6eca9cc
Source noteuspto-grants-1981_08