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HRID 339314Erstellt: 25. Oktober 2026

Tris(hydroxymethyl)aminomethane → N-(2,3-dimethylcyclohexyl)benzo[d][1,3]dioxole-5-carboxamide

https://huagongshe.com/reaction/339314

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTris(hydroxymethyl)aminomethaneHCID 6503—
Edukt1,3-Benzodioxole-5-carboxylic acidHCID 7196—
Edukt2,3-DimethylcyclohexylamineHCID 123507—
EduktCarbodiimideHCID 160435—
EduktHCID 178418300HCID 178418300—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelAcetonitrileHCID 6342—
LösungsmittelAcetonitrile methylene chlorideHCID 21877088—
ProduktN-(2,3-dimethylcyclohexyl)benzo[d][1,3]dioxole-5-carboxamideHCID 17479454—

Reaktionsschritte

2,3-dimethylcyclohexanamine (20 μmol) and benzo[d][1,3]dioxole-5-carboxylic acid (1.1 eq) were each dissolved in acetonitrile/dichloromethane (200 μL, 2:1). PS-Carbodiimide resin (2 eq) was loaded into a 1.2 mL 96 well Greiner plate, followed by the addition of amine and acid solutions. Hydroxybenzotriazole (1.1 eq) was dissolved in DMF (100 mL) and was added into the reaction well. The reaction was shaken overnight at room temperature. Once the reaction was completed, PS-Trisamine resin (1.5 eq) was added into the reaction mixture and the solution was allowed to shake overnight at room temperature. Acetonitrile (200 mL) was added into the reaction well, and the top clear solution was transferred into a new plate. The solution was evaporated to give N-(2,3-dimethylcyclohexyl)benzo[d][1,3]dioxole-5-carboxamide. MS (M+H, 276.20).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08895050B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-214d46e93fd848efac87ce532459a3b5
Quellennotizuspto-grants-2014_11