HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1163363Generated: October 28, 2026
Chlorotrimethylsilane → HCID 87333265, compound
https://huagongshe.com/reaction/1163363
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 7-Chloro-1-cyclopropyl-6-fluoro-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylic acid | HCID 11055142 | — |
| Reactant | HCID 86597771 | HCID 86597771 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 87333265 | HCID 87333265 | 29.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07820823B2 |
|---|
| Source dataset | uspto-grants-2010_10 |
|---|
| ORD ID | ord-7677f4b222f54be88692b3c67bb831af |
|---|
| Source note | uspto-grants-2010_10 |
|---|