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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 421227Erstellt: 27. Oktober 2026

Dichloromethane → Diisopropylethylamine

https://huagongshe.com/reaction/421227

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDichloromethaneHCID 6344—
EduktDiisopropylethylamineHCID 81531—
EduktO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Edukt4-(tert-Butoxycarbonyl)morpholine-3-carboxylic acidHCID 2760133—
ProduktDiisopropylethylamineHCID 81531—
ProduktMethyl D-alaninate hydrochlorideHCID 11182647—
Produkt(3R)-3-methyltetrahydro-2H-pyrazino[1,2-a]pyrazine-1,4(3H,6H)-dioneHCID 59215897—

Reaktionsschritte

To a solution of N-boc-morpholine-3-carboxylic acid (2 g, 9.379 mmol) in 60 mL of dichloromethane and was added TBTU (3.313 g, 10.32 mmol) and diisopropylethyl amine (1.96 mL, 11.25 mmol). The reaction was stirred for 30 min. In the meantime, a solution of D-alanine methyl ester hydrochloride (1.93 g, 18.76 mmol) and diisopropylethylamine (3.27 mL, 18.76 mmol) in 20 mL of dichloromethane was prepared and finally added to the reaction mixture. The reaction was left stirring at room temperature for 2 h. UPLC-MS analysis showed the expected product (peak at 0.60 min, m/z=317 (M+1), 261 (M−t-Bu+1), 217 (M−Boc+1)). The reaction was diluted with dichloromethane and extracted with sat. NaHCO3, dried (Na2SO4), and the solvent removed. The crude (5.56 g) was taken to the next step without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08097618B2
Quelldatensatzuspto-grants-2012_01
ORD IDord-fca0426383df493bb055573c88de7bea
Quellennotizuspto-grants-2012_01