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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1163363Generated: October 28, 2026

Chlorotrimethylsilane → HCID 87333265, compound

https://huagongshe.com/reaction/1163363

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 86597771HCID 86597771—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 87333265HCID 8733326529.8%

Reaction Conditions

Temperature150 °C

Reaction Steps

A mixture of 100 mg [(5S)-3-(3-fluoro-4-piperazin-1-yl-phenyl)-2-oxo-oxazolidin-5-ylmethyl]-thiourea (0.28 mmol), 87.98 mg 7-chloro-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylic acid (0.31 mmol), 71.57 μl trimethylchlorosilane (0.56 mmol) and 118.31 μl triethylamine (1.4 mmol) in acetonitrile was stirred in a micro wave oven for 8 min at 150° C. The reaction mixture was diluted with water and the solid filtered. The solid was purified by chromatography using a 95/5 dichloromethane/methanol mixture with 1% acetic acid as eluent to leave 50 mg of an oily residue which was crystallized from a ETOAC/hexane mixture.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820823B2
Source datasetuspto-grants-2010_10
ORD IDord-7677f4b222f54be88692b3c67bb831af
Source noteuspto-grants-2010_10