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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1290255Erstellt: 25. Oktober 2026

Diisopropylcarbodiimide → HCID 18923868, Verbindung

https://huagongshe.com/reaction/1290255

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylcarbodiimideHCID 12734—
Edukt1-Hydroxybenzotriazole hydrateHCID 2796029—
Edukt5-Methoxyindole-3-butyric acidHCID 11241777—
Edukt2,3-Dihydro-7-hydroxy-1,4-benzodioxin-2-methanamine hydrochlorideHCID 18923890—
LösungsmittelDimethylformamideHCID 6228—
ProduktHCID 18923868HCID 1892386865,4%

Reaktionsschritte

5-Methoxyindole-3-butyric acid (1.5 g, 6.4 mmole), 1-hydroxybenzotriazole hydrate (1.0 g, 7.7 mmole) and 1,3-diisopropylcarbodiimide (2.4 ml, 15.4 mmole) were combined in 150 ml of DMF and stirred at room temperature for 2 hours under a nitrogen atmosphere. To this was added dropwise 7-hydroxy-2,3-dihydro-1,4-benzodioxin-2-methanamine hydrochloride (1.4 g, 6.4 mmole) in 50 ml of DMF and the mixture was further stirred for 24 hours. The solvent was removed and the residue partitioned between dichloromethane and water. The separated dichloromethane layer was dried over anhydrous sodium sulfate, filtered and concentrated in vacuum. The residue was chromatographed on a silica gel column using first ethyl acetate and then 5% methanol in ethyl acetate as eluants. Evaporation of product-containing fractions gave 1.6 g (63%) of the desired product, (7-hydroxy-2,3-dihydro-benzo[1,4]dioxin-2-ylmethyl)-4-(5-methoxy-1H-indol-3-yl)-butanamide, as an oily solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05750724
Quelldatensatzuspto-grants-1998_05
ORD IDord-c882b072f41e44a080ce475d587f4cc2
Quellennotizuspto-grants-1998_05