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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2075772Erstellt: 24. Oktober 2026

Acetic Acid → HCID 178452458, Verbindung

https://huagongshe.com/de/reaction/2075772

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktDiisopropylcarbodiimideHCID 12734—
EduktLithium hydroxide, monohydrateHCID 168937—
Edukt(3S)-4-(tert-Butoxycarbonyl)morpholine-3-carboxylic acidHCID 1512537—
Edukt2-[4-(4-Amino-phenylethynyl)-1H-pyrazol-3-yl]-4-chloro-phenolHCID 178507548—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelEthyl AcetateHCID 8857—
ProduktHCID 178452458HCID 17845245871,4%

Reaktionsschritte

To a solution of compound 24A (930 mg, 3.0 mmol) and (S)-morpholine-3,4-dicarboxylic acid 4-tert-butyl ester (19A, 2.09 g, 9.0 mmol) in anhydrous dichloromethane (20 mL) was added N,N′-diisopropylcarbodiimide (DIPC, 1.4 mL, 9.0 mmol). The reaction mixture was stirred at rt overnight. Solvent was removed. To the residua were added THF (20 mL) and methanol (20 mL) and a solution of LiOH.H2O (1.0 g, 23.84 mmol) in water (10 mL). The mixture was stirred at rt for 2 h. It was then neutralized with acetic acid (1.36 mL, 23.84 mmol). The mixture was diluted with ethyl acetate (˜100 mL), washed with brine, and dried over sodium sulfate. It was filtered, concentrated and filtered again to remove diisopropylurea. The filtrate was purified with silica column chromatography eluting with dichloromethane/ethyl acetate (v/v 5/1, 3/1, 2/1, 1/1) to provide the title compound (28A, 1.12 g) as a yellowish solid in 71.3% yield. LCMS (ESI) m/z 587.15 (MNa+), 521.05 (MH+), 421.06; HPLC: tR=5.32 min.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07923004B2
Quelldatensatzuspto-grants-2011_04
ORD IDord-adbb3e7842b04fda9aaad5fd9a282c7c
Quellennotizuspto-grants-2011_04