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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 448271Erstellt: 24. Oktober 2026

Diisopropylethylamine → HCID 178480346, Verbindung

https://huagongshe.com/de/reaction/448271

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
EduktO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Edukt4-Piperidinecarboxylic acid, 1-methyl-, hydrochloride (1:1)HCID 2760043—
EduktDichloromethane methanol ammonium hydroxideHCID 21896990—
EduktHCID 68649268HCID 68649268—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelEthyl acetate hexaneHCID 21226206—
ProduktHCID 178480346HCID 17848034669,3%

Reaktionsschritte

Ethyl 3-[(4-fluorobenzoyl)amino]-6,6-dimethyl-5,6-dihydropyrrolo[3,4-c]pyrazole-1(4H)-carboxylate hydrochloride (0.5 g, 1.3 mmol), in dichloromethane (25 ml), was treated with N,N-diisopropylethylamine (1.13 ml, 6.5 mmol, 5 eq) and TBTU (0.542 g, 1.69 mmol, 1.3 eq), at room temperature for 1 hour, and then 1-methyl-piperidine-4-carboxylic acid hydrochloride (0.29 g, 1.61 mmol, 1.2 eq) was added. The reaction was stirred overnight (TLC: CH2Cl2/MeOH 90/10). The solution was washed with saturated sodium hydrogencarbonate aqueous solution and brine, the organic phase was dried over sodium sulfate and concentrated. The residue was dissolved in methanol (16 ml), treated with TEA (2 ml, 14.3 mmol, 11 eq) and stirred overnight at room temperature. (TLC: CH2Cl2/MeOH/NH4OH 90/10/1). After evaporation, the solid was purified by flash chromatography (eluent: CH2Cl2/MeOH/NH4OH 90/10/2). The solid was treated with diisopropylether and filtered to afford 0.36 g of the title compound in 69% yield.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08481585B2
Quelldatensatzuspto-grants-2013_07
ORD IDord-3963e645ccbc4f95ad959c0173a1757f
Quellennotizuspto-grants-2013_07