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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1753913Erstellt: 24. Oktober 2026

Diisopropylethylamine → HCID 70816785, Verbindung

https://huagongshe.com/de/reaction/1753913

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Edukttrans-2-Aminomethyl-1-cyclohexanolHCID 2724658—
Edukt1-Hydroxybenzotriazole hydrateHCID 2796029—
EduktHCID 70817044HCID 70817044—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelEthyl AcetateHCID 8857—
LösungsmittelAmmonium ChlorideHCID 25517—
ProduktHCID 70816785HCID 7081678563%

Reaktionsschritte

To a solution of 2-isopropyl-4-methyl-6-morpholin-4-yl-pyridine-3-carboxylic acid (synthesized similar to the methods described in sections a) to d) of example X1) (0.20 g, 0.76 mmol) in dichloromethane (15 ml) are added N-ethyl-diisopropylamine (0.32 ml, 0.89 mmol), 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride (0.17 g, 0.91 mmol), and 1-hydroxybenzotriazole hydrate (0.02 g, 0.15 mmol). The mixture is stirred for 15 min at RT, and then cooled to 0° C., before (1R,2S)-2-(aminomethyl)cyclohexanol (0.09 g, 0.76 mmol) is added and stirring is continued for 18 h. After completion of the reaction, the mixture is diluted with ethyl acetate and 10% aqueous ammonium chloride. The organic layer is separated and washed with saturated sodium hydrogencarbonate solution and brine, dried over magnesium sulphate and evaporated to dryness. The crude product is purified by flash chromatography (silica gel, 50% ethyl acetate/cyclohexane) to yield N-[[(1S,2R)-2-hydroxy-cyclohexyl]-methyl]-2-isopropyl-4-methyl-6-morpholin-4-yl-pyridine-3-carboxylic acid amide (example X7) (0.18 g, 0.48 mmol, 63%). [M+H]+376.3.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09168259B2
Quelldatensatzuspto-grants-2015_10
ORD IDord-eabe245b6376419ebe490432d8fc37e4
Quellennotizuspto-grants-2015_10