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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2387570Generated: November 1, 2026

Chlorotrimethylsilane → HCID 69121786, compound

https://huagongshe.com/reaction/2387570

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantTriethylamineHCID 8471—
Reactant7-Chloro-1-cyclopropyl-6-fluoro-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylic acidHCID 11055142—
ReactantHCID 57754803HCID 57754803—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 69121786HCID 69121786—

Reaction Conditions

Temperature150 °C

Reaction Steps

A suspension of 179 mg N-{(5S)-3-[4-(Azetidin-3-ylmethoxy)-3-fluoro-phenyl]-2-oxo-oxazolidin-5-yl methyl}-acetamide (MW: 337.35, 0.31 mmol), 100 mg 7-chloro-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-1,8-Naphthyridine-3-carboxylic acid (MW: 282.66, 0.25 mmol), 0.134 ml trimethylchlorosilane (MW: 108.64, d=0.859, 1.059 mmol) and 0.197 ml triethylamine (MW: 101.19, d=0.726, 1.41 mmol) in 2 ml N-methyl-pyrrolidin-2-one was heated under stirring in a micro wave oven at 150° C. for 7 min. The N-methyl-pyrrolidin-2-one was evaporated, the residue was purified by chromatography. Yield: 82 mg, 40%. MS: 583.5 (M+H)+, Method ESI+. Molecular Weight=584

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08268812B2
Source datasetuspto-grants-2012_09
ORD IDord-c9efae6ce65e4745b5bf75c0e9aba5ac
Source noteuspto-grants-2012_09