Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2387569Generated: October 31, 2026

Chlorotrimethylsilane → HCID 69121517, compound

https://huagongshe.com/reaction/2387569

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 57754854HCID 57754854—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 69121517HCID 69121517—

Reaction Conditions

Temperature150 °C

Reaction Steps

A suspension of 100 mg N-{(5S)-3-[4-(Azetidin-3-yloxy)-3-fluoro-phenyl]-2-oxo-oxazolidin-5-yl methyl}-acetamide (MW: 323.32, 0.31 mmol), 73 mg 7-chloro-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-1,8-Naphthyridine-3-carboxylic acid (MW: 282.66, 0.25 mmol), 0.066 ml trimethylchlorosilane (MW: 108.64, d=0.859, 0.51 mmol) and 0.108 ml triethylamine (MW: 101.19, d=0.726, 0.77 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: 55 mg, 30%. MS: 570.5 (M+H)+, Method ESI+. Molecular Weight=570

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08268812B2
Source datasetuspto-grants-2012_09
ORD IDord-25f7be45a0e5405895ea3b647ac1192b
Source noteuspto-grants-2012_09