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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 251382Erstellt: 26. Oktober 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → Ethyl 3-{[2-(4-morpholinyl)ethyl]oxy}benzoate

https://huagongshe.com/reaction/251382

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Edukttert-Butyl carbazateHCID 70091—
Edukt1-HydroxybenzotriazoleHCID 75771—
Edukt3-(5-amino-4-benzoyl-1H-pyrazol-1-yl)-4-methylbenzoic acidHCID 11209438—
EduktSodium chloride; waterHCID 57417360—
LösungsmittelDimethylformamideHCID 6228—
ProduktEthyl 3-{[2-(4-morpholinyl)ethyl]oxy}benzoateHCID 5808903926%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To DMF (10 mL) at rt was added 3-(5-amino-4-benzoyl-pyrazol-1-yl)-4-methyl-benzoic acid 1 (0.50 g, 1.56 mmol, 1.0 eq), t-butylcarbazate (0.206 g, 1.56 mmol, 1.0 eq), EDCI (0.313 g, 1.63 mmol, 1.05 eq) and HOBt (0.238 g, 1.56 mmol, 1.0 eq). The reaction was stirred for 19 h, poured into brine (100 mL) and extracted with EtOAc (2×20 mL). The organic extracts were combined were washed with brine (1×20 mL). The brine layer was separated and extacted with EtOAc (1×10 mL). All organic extracts were combined dried over Na2SO4, filtered and concentrated in vacuo. This material was dissolved in CH2Cl2 (10 mL) and cooled to 0° C. TFA (3 mL) was added and the reaction mixture allowed to warm to rt over 2 h. The solvent was removed in vacuo to give crude solid which was triturated with EtOAc/ether (1/1) giving 2 (180 mg, 26%)as a light tan in color solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07863314B2
Quelldatensatzuspto-grants-2011_01
ORD IDord-01c92dc9ae754fbfa8ce639352e63b35
Quellennotizuspto-grants-2011_01