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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1372644Erstellt: 25. Oktober 2026

5-Fluoro-o-tolyl Isothiocyanate → Methyl (2-(5-fluoro-2-methylphenylamino)-7-fluoro-6-benzoxazolyl)acetate

https://huagongshe.com/reaction/1372644

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt5-Fluoro-o-tolyl IsothiocyanateHCID 519443—
EduktMethyl (4-amino-2-fluoro-3-hydroxyphenyl)acetateHCID 17859032—
LösungsmittelMethanolHCID 887—
ProduktMethyl (2-(5-fluoro-2-methylphenylamino)-7-fluoro-6-benzoxazolyl)acetateHCID 4460752156%

Reaktionsschritte

In methanol (30 ml) was dissolved methyl (4-amino-2-fluoro-3-hydroxyphenyl)acetate (1.0 g, 5.02 mmol). To the resulting solution was added 5-fluoro-2-methylphenyl isothiocyanate (1.0 g, 5.98 mmol). After the resulting mixture was stirred at room temperature for 5 days, mercuric oxide (yellow) (1.14 g, 4.36 mmol) was added thereto. The mixture was stirred at 70° C. for 6 hours. After cooling to room temperature, the reaction mixture was filtered through Celite and washed with methanol. The filtrate was distilled under reduced pressure to remove the solvent. The residue was purified by chromatography on a silica gel column, whereby from chloroform/ethyl acetate (30/1, v/v) eluate fractions, methyl (2-(5-fluoro-2-methylphenylamino)-7-fluoro-6-benzoxazolyl)acetate (810 mg, 56% (2 steps)) was obtained as a pink solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07157487B2
Quelldatensatzuspto-grants-2007_01
ORD IDord-672c550ec85c4431afa5341f70e99fc0
Quellennotizuspto-grants-2007_01