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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 852798Erstellt: 24. Oktober 2026

Triethylamine → HCID 178453727, Verbindung

https://huagongshe.com/de/reaction/852798

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Edukt1-HydroxybenzotriazoleHCID 75771—
Edukt4-(2-((tert-Butoxycarbonyl)amino)ethoxy)benzoic acidHCID 2755997—
EduktHCID 178422083HCID 178422083—
LösungsmittelDichloromethaneHCID 6344—
ProduktHCID 178453727HCID 178453727412,1%

Reaktionsschritte

A mixture of 2-((2S)-bicyclo[2.2.1]heptan-2-ylamino)-5-methyl-5-(piperidin-4-ylmethyl)thiazol-4(5H)-one (534 mg, 1.66 mmol), 4-[2-(Boc-amino)ethyloxy]-benzoic acid (NeoMPS, 701 mg, 2.49 mmol), EDCI (Aldrich, 637 mg, 3.32 mmol, 2.0 eq), HOBt (Aldrich, 45 mg, 0.332 mmol, 0.2 eq) and triethylamine (Aldrich, 336 mg, 3.32 mmol, 2.0 eq) in CH2Cl2 (10 mL) was stirred at room temperature for ca. 18 h. The reaction was quenched with saturated NaHCO3 (100 mL), and the crude product was extracted with CH2Cl2 (3×100 mL). The combined organic extracts were washed with brine, dried over Na2SO4, filtered, and concentrated. Flash column chromatography (silica gel, 0-5% MeOH in CH2Cl2) afforded the title compound as a white solid (800 mg). MS (ESI, pos. ion) m/z: 585 (M+H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07253196B2
Quelldatensatzuspto-grants-2007_08
ORD IDord-ea66cf13d49c4281992f9802fc79f921
Quellennotizuspto-grants-2007_08