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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 974948Erstellt: 25. Oktober 2026

4-Methylmorpholine → Boc-3-cyano-(L)-phenylalanine-4-methylsulfonylpiperazide

https://huagongshe.com/reaction/974948

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-MethylmorpholineHCID 7972—
EduktDicyclohexylcarbodiimideHCID 10868—
Edukt1-HydroxybenzotriazoleHCID 75771—
Edukt(2S)-2-{[(tert-butoxy)carbonyl]amino}-3-(3-cyanophenyl)propanoic acidHCID 2734498—
Edukt1-Methanesulfonylpiperazine hydrochlorideHCID 16265612—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktBoc-3-cyano-(L)-phenylalanine-4-methylsulfonylpiperazideHCID 131719883—

Reaktionsschritte

4.92 g (24.5 mmol) of 1-methylsulfonylpiperazine hydrochloride and 2.7 ml (24.5 mmol) of NMM was dissolved in 50 ml of DMF. After addition of 4 g (29.6 mmol) of HOBt and a solution of 5.93 g (20.4 mmol) of Boc-3-cyano-(L)-phenylalanine in 200 ml of THF, the mixture was cooled to O° C. 5.1 g (24.7 mmol) of DCC were added and the mixture was stirred for 48 hours at room temperature. Afterwards, the precipitated dicyclohexyl urea was filtered off, the THF moiety of the solution evaporated under reduced pressure, filtered and the filtrate poured into a mixture of 100 ml of 5% sodium bicarbonate solution and 200 ml of ice water. The formed precipitate was filtered off, washed with water, dissolved in methanol and the solvent was evaporated under reduced pressure. To remove the still present water, a co-distillation with toluene/isopropanol was performed several times. The only slightly impure product was processed in this form. Yield: 7.9 g (89%)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05607937
Quelldatensatzuspto-grants-1997_03
ORD IDord-4bd99622e3064d3ea1dfc1bbd73f19fe
Quellennotizuspto-grants-1997_03