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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2366444Erstellt: 24. Oktober 2026

4-Toluenesulfonyl chloride → YHO-13351 free base

https://huagongshe.com/de/reaction/2366444

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Toluenesulfonyl chlorideHCID 7397—
Edukt(Z)-2-(3,4-dimethoxyphenyl)-3-(5-(4-hydroxypiperidin-1-yl)thiophen-2-yl)acrylonitrileHCID 16757522—
EduktGlycine, N,N-diethyl-, sodium salt (1:1)HCID 23670834—
LösungsmittelPyridineHCID 1049—
ProduktYHO-13351 free baseHCID 1196478575%

Reaktionsschritte

Compound 6 (3.70 g) was dissolved in pyridine (100 mL), and N,N-diethylglycin sodium salt (7.66 g) was added to the solution, followed by stirring at room temperature for 1 hour. Subsequently, p-toluenesulfonyl chloride (9.43 g) was added to the mixture, followed by stirring under reflux for 12 hours. After completion of reaction, the solvent was evaporated under reduced pressure. Chloroform (1,000 mL) was added to the residue, and the mixture was washed with water three times. The pH of the aqueous layer was checked by use of a pH testpaper, and adjusted to 4 to 5 with 1N aqueous hydrochloric acid. The organic layer was dried over sodium sulfate anhydrate, and the solvent was evaporated to dryness. The residue was purified by silica gel column chromatography (CHCl3-Hexane), to thereby yield the target product (yield: 3.62 g, 75%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08697742B2
Quelldatensatzuspto-grants-2014_04
ORD IDord-b417832a5a124c44916a2fef3da95545
Quellennotizuspto-grants-2014_04