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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 448781Erstellt: 24. Oktober 2026

L-Methioninol → N-[[1-[[[4-[2-(4-Methyl-1-piperazinyl)-4-thiazolyl]phenyl]carbonyl]amino]cyclohexyl]carbonyl]-L-methioninol

https://huagongshe.com/de/reaction/448781

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktL-MethioninolHCID 2724404—
Edukt2-[4-[2-(4-Methyl-1-piperazinyl)-4-thiazolyl]phenyl]-3-oxa-1-azaspiro[4.5]dec-1-en-4-oneHCID 57672803—
LösungsmittelDimethylformamideHCID 6228—
ProduktN-[[1-[[[4-[2-(4-Methyl-1-piperazinyl)-4-thiazolyl]phenyl]carbonyl]amino]cyclohexyl]carbonyl]-L-methioninolHCID 5767285086%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

100 mg (0.74 mmol) of L-methioninol was added to a solution of 250 mg (0.68 mmol) of 2-[4-[2-(4-methyl-1-piperazinyl)-4-thiazolyl]phenyl]-3-oxa-1-azaspiro[4.5]dec-1-en-4-one in 20 ml of dimethylformamide. After the mixture was stirred at 80° C. for 15 hours, the reaction solution was concentrated under reduced pressure, ethyl acetate was added thereto, and the mixture was successively washed with water, a saturated aqueous sodium hydrogencarbonate solution and saturated brine, followed by drying with anhydrous sodium sulfate. After the solvent was distilled off under reduced pressure, and diisopropyl ether was added to the residue to wash the crystal to obtain 319 mg (86%) of the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08481725B2
Quelldatensatzuspto-grants-2013_07
ORD IDord-fa3326ca2b774c608a65c4913075f958
Quellennotizuspto-grants-2013_07