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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 341271Erstellt: 24. Oktober 2026

Triethylamine → 3-{[4-(Methylthio)-1,3-thiazol-2-yl]carbamoyl}phenyl acetate

https://huagongshe.com/de/reaction/341271

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt3-(Chlorocarbonyl)phenyl acetateHCID 12998558—
Edukt4-(Methylthio)-1,3-thiazol-2-amineHCID 55285798—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3-{[4-(Methylthio)-1,3-thiazol-2-yl]carbamoyl}phenyl acetateHCID 57571980121,4%

Reaktionsschritte

Into a solution of 511 (0.815 g, 4.10 mmol) and dry THF (25.0 mL) was added triethylamine (0.572 mL, 4.10 mmol), followed by a solution of the 508 (0.500 g, 3.42 mmol) dissolved in dry THF (10.0 mL). The reaction was stirred at room temperature. After stirring overnight, the reaction was concentrated in vacuo. The residue was dissolved in ethyl acetate and washed once with water, three times with saturated aqueous. sodium bicarbonate solution, and once with brine. The ethyl acetate solution was dried over anhydrous sodium sulfate and concentrated in vacuo to give crude 85 (1.28 g, >100%) as a red foam. The crude product was dissolved in dichloromethane. Silica gel was added to the dichloromethane solution and the suspension was concentrated in vacuo. The residue was loaded on top of a 90 g silica gel cartridge and eluted down the column using a solution of 20% ethyl acetate in hexane. Appropriate fractions of the major product were combined and concentrated in vacuo to give 85 (0.614 g, 58%) as a tan solid. This material was used in the next step without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08895752B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-87b97b340bae4b149be2b83570b9d85c
Quellennotizuspto-grants-2014_11