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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1075185Erstellt: 25. Oktober 2026

Chlorotrimethylsilane → alpha-(4-Ethyl-2,3-dioxo-1-piperazinecarboxamido)-2-furylacetic acid

https://huagongshe.com/reaction/1075185

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChlorotrimethylsilaneHCID 6397—
EduktTriethylamine hydrochlorideHCID 11130—
Edukt4-Ethyl-2,3-dioxopiperazinecarbonyl chlorideHCID 108813—
Edukt2-Amino-2-(furan-2-yl)acetic acidHCID 298385—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelTriethylamineHCID 8471—
Produktalpha-(4-Ethyl-2,3-dioxo-1-piperazinecarboxamido)-2-furylacetic acidHCID 1557335285,6%

Reaktionsschritte

To an ice-cooled suspension of 2.55 g of DL-α-amino-2-furylacetic acid in 35 ml of methylene chloride was added 4.81 ml of trimethylchlorosilane. To the resulting mixture was added dropwise 5.04 ml of triethylamine over a period of 10 minutes at 5° to 10° C. The reaction was allowed to proceed at 15° to 20° C. for one hour. To the reaction mixture was added over a period of 15 minutes at 5° to 10° C. 7.01 g of a mixture of 4-ethyl-2,3-dioxo-1-piperazinecarbonyl chloride and triethylamine hydrochloride, said mixture containing 58.02% of the former. The reaction was allowed to proceed at 10° to 15° C. for one hour. After addition of 20 ml of water, the reaction mixture was stirred at room temperature for one hour, then at 5° to 7° C. for 30 minutes. The precipitated crystals were collected by filtration, washed with 5 ml of methylene chloride and 5 ml of water in this order, and then dried to obtain 4.75 g of DL-α-(4-ethyl-2,3-dioxo-1-piperazinecarboxamido)-2-furylacetic acid, m.p. 179°-181° C. (decomp.), yield 85.6%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04395412
Quelldatensatzuspto-grants-1983_07
ORD IDord-817204799dfb4e57a572672069df7a31
Quellennotizuspto-grants-1983_07