Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1085088Generated: October 23, 2026

N-methyl-N-(trimethylsilyl)trifluoroacetamide → (6R,7R)-7-[[(2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-methoxyiminoacetyl]amino]-3-(iodomethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid

https://huagongshe.com/en/reaction/1085088

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-methyl-N-(trimethylsilyl)trifluoroacetamideHCID 32510—
ReactantTrimethylsilyl iodideHCID 85247—
ReactantCefotaximeHCID 5742673—
SolventDichloromethaneHCID 6344—
Product(6R,7R)-7-[[(2Z)-2-(2-amino-1,3-thiazol-4-yl)-2-methoxyiminoacetyl]amino]-3-(iodomethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acidHCID 14252931—

Reaction Steps

7β-[(Z)-2-(2-Aminothiazol-4-yl)-2-methoxyiminoacetamido]-3-acetoxymethyl-3-cephem-4-carboxylic acid (977 mg) was suspended in methylene chloride (16 ml), followed by an addition of N-methyl-N-(trimethylsilyl) trifluoroacetamide (1350 μl). The resulting mixture was stirred at room temperature for 1 hour. After ice-cooling, iodotrimethylsilane (810 μl) was added and the resulting mixture was stirred for 15 minutes. The reaction mixture was concentrated under reduced pressure to obtain the silylated derivative of 7β-[(Z)-2-(2-aminothiazol-4-yl)-2-methoxyiminoacetamido]-3-iodomethyl-3-cephem-4-carboxylic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05008260
Source datasetuspto-grants-1991_04
ORD IDord-e8783b6d6eb54542a12dccd68b8cb1ca
Source noteuspto-grants-1991_04