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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 323709Erstellt: 23. Oktober 2026

4-Methylmorpholine → HCID 69861742, Verbindung

https://huagongshe.com/de/reaction/323709

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-MethylmorpholineHCID 7972—
Edukt1H-Indole-2-carboxylic acid, 1-methyl-HCID 27695—
Eduktphenylalaninol, (S)-HCID 447213—
Edukt1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Edukt1-Hydroxybenzotriazole hydrateHCID 2796029—
LösungsmittelMethanolHCID 887—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelDichloromethaneHCID 6344—
ProduktHCID 69861742HCID 6986174268,1%

Reaktionsschritte

To a stirred solution of 1-methyl-2-indolecarboxylic acid (100 mg, 0.57 mmol) in methylene chloride (1 mL) was added N-methylmorpholine (0.063 mL, 0.57 mmol) followed by (S)-(−)-2-amino-3-phenyl-1-propanol (86 mg, 0.57 mmol), 1-hydroxybenzotriazole hydrate (81 mg, 0.60 mmol), and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (120 mg, 0.63 mmol). The resulting mixture was stirred at room temperature for 20 h. The reaction was diluted with methylene chloride and washed sequentially with 10% citric acid, saturated NaHCO3, water, and brine. The organic layer was dried over Na2SO4 and concentrated in vacuo to give a crude oil. Trituration of the crude oil with methanol and diethyl ether afforded the title compound (68%, 119.7 mg) as an off-white solid. MS (ES) m/e 309.4 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06214856B1
Quelldatensatzuspto-grants-2001_04
ORD IDord-ba43aa1208ed46849711ebd9f4436e12
Quellennotizuspto-grants-2001_04